[
  {
    "brand": "Salton, Inc.",
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    "device_name": "REJUVENIQUE MODEL #RJV10",
    "product_code": "NFO",
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    "decision_code": "SESE",
    "applicant": "Salton, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K011935",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
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  {
    "brand": "Facemaster of Beverly Hills, Inc.",
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    "device_name": "FACEMASTER FACIAL TONING SYSTEM",
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    "k_number": "K040871",
    "decision_date": "2005-06-01",
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    "applicant": "Facemaster of Beverly Hills, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K040871",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
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  {
    "brand": "Palomar Medical Technologies, Inc.",
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    "device_name": "ABC HAIR REMOVAL SYSTEM",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K060839",
    "decision_date": "2006-12-07",
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    "applicant": "Palomar Medical Technologies, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K060839",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
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  },
  {
    "brand": "Light Bioscience, LLC",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "GENTLEWAVES CONSUMER LED PHOTOMODULATION DEVICE",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K062991",
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    "applicant": "Light Bioscience, LLC",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K062991",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
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  },
  {
    "brand": "Neuro Resource Group, Inc.",
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    "device_name": "INTERX 1000/DERMA 200 STIMULATOR FOR COSMETIC USE",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K070217",
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    "decision_code": "SESE",
    "applicant": "Neuro Resource Group, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K070217",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Isomers Laboratories, Inc.",
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    "device_name": "NUTRITONE FACIAL BEAUTY SYSTEM",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K070250",
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    "decision_code": "SESE",
    "applicant": "Isomers Laboratories, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K070250",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Fatrotek S.R.L.",
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    "device_name": "RUGALIFT, MODEL# V.2.1",
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    "k_number": "K071573",
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    "applicant": "Fatrotek S.R.L.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K071573",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
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  },
  {
    "brand": "Carol Cole Company",
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    "device_name": "NUFACE, MODEL NU-4003",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K072260",
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    "decision_code": "SESE",
    "applicant": "Carol Cole Company",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K072260",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Photo Therapeutics, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "OMNILUX NEW-U",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K072459",
    "decision_date": "2008-03-03",
    "decision_code": "SESE",
    "applicant": "Photo Therapeutics, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K072459",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Photo Therapeutics, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "OMNILUX CLEAR-U",
    "product_code": "OLP",
    "category": "acne-light",
    "k_number": "K081307",
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    "decision_code": "SESE",
    "applicant": "Photo Therapeutics, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K081307",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OLP%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Clrs Technology Corporation",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "CLARO",
    "product_code": "OLP",
    "category": "acne-light",
    "k_number": "K090744",
    "decision_date": "2010-04-15",
    "decision_code": "SESE",
    "applicant": "Clrs Technology Corporation",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K090744",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OLP%22&limit=1000&skip=0&sort=decision_date%3Adesc",
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  },
  {
    "brand": "Ps Advanced Engineering",
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    "device_name": "STAR-LITE -LM, MODEL SL8809",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K092460",
    "decision_date": "2010-03-05",
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    "applicant": "Ps Advanced Engineering",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K092460",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
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  },
  {
    "brand": "Silver Bay, LLC",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "QUASAR BLUE LIGHT THERAPY SYSTEM",
    "product_code": "OLP",
    "category": "acne-light",
    "k_number": "K093963",
    "decision_date": "2010-08-27",
    "decision_code": "SESE",
    "applicant": "Silver Bay, LLC",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K093963",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OLP%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Led Intellectual Properties, LLC",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LIGHTSTIM ANTI-WRINKLE OTC MODEL AAL OTC",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K101190",
    "decision_date": "2010-07-01",
    "decision_code": "SESE",
    "applicant": "Led Intellectual Properties, LLC",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K101190",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Led Technologies, LLC",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "DPL NUVE",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K101382",
    "decision_date": "2010-11-09",
    "decision_code": "SESE",
    "applicant": "Led Technologies, LLC",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K101382",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Radiancy (Israel) , Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "NO!NO! SKIN",
    "product_code": "OLP",
    "category": "acne-light",
    "k_number": "K102477",
    "decision_date": "2010-10-04",
    "decision_code": "SESE",
    "applicant": "Radiancy (Israel) , Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K102477",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OLP%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Daka International , Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "THE BUZZ FACIAL TONING SYSTEM",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K102494",
    "decision_date": "2011-12-09",
    "decision_code": "SESE",
    "applicant": "Daka International , Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K102494",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
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  },
  {
    "brand": "Bio-Medical Research, Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "BMR FACE",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K103031",
    "decision_date": "2011-11-10",
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    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K103031",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
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  {
    "brand": "Home Skinovations , Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "SILK'N FLASH N GO",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K103184",
    "decision_date": "2010-11-10",
    "decision_code": "SESE",
    "applicant": "Home Skinovations , Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K103184",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
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  {
    "brand": "Carol Cole Company",
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    "device_name": "NUFACE PLUS",
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    "category": "microcurrent",
    "k_number": "K103472",
    "decision_date": "2011-11-07",
    "decision_code": "SESE",
    "applicant": "Carol Cole Company",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K103472",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
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  {
    "brand": "Home Skinovations , Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "SILK'N FX",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K110301",
    "decision_date": "2011-08-19",
    "decision_code": "SESE",
    "applicant": "Home Skinovations , Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K110301",
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    "brand": "Pharos Life Corporation",
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    "device_name": "TANDA MAX OTC SYSTEM",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K110735",
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    "decision_code": "SESE",
    "applicant": "Pharos Life Corporation",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K110735",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
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    "brand": "Silver Bay, LLC",
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    "device_name": "QUASAR CALYPSO",
    "product_code": "OLP",
    "category": "acne-light",
    "k_number": "K111286",
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    "applicant": "Silver Bay, LLC",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K111286",
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    "brand": "Cynosure, Inc.",
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    "device_name": "ILUMINAGE DIODE LASER",
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    "category": "led",
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    "applicant": "Cynosure, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K111454",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
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    "brand": "Clearflash Technologies, Inc.",
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    "device_name": "CLEARFLASH AC2100 COSMETIC SYSTEM",
    "product_code": "OLP",
    "category": "acne-light",
    "k_number": "K111937",
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    "decision_code": "SESE",
    "applicant": "Clearflash Technologies, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K111937",
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  },
  {
    "brand": "Johari Digital Healthcare , Ltd.",
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    "device_name": "ULTRA BEAUTY",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K112351",
    "decision_date": "2012-03-30",
    "decision_code": "SESE",
    "applicant": "Johari Digital Healthcare , Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K112351",
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    "brand": "Silver Bay, LLC",
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    "device_name": "C100 WRINKLE REDUCTION DEVICE",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K112362",
    "decision_date": "2012-08-14",
    "decision_code": "SESE",
    "applicant": "Silver Bay, LLC",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K112362",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
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  },
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    "brand": "Pain Relief Technologies",
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    "device_name": "ELECTROPULSE-COSMETIC",
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    "k_number": "K113724",
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    "applicant": "Pain Relief Technologies",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K113724",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Leto Enterprise , Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "AGELESS WONDER FACIAL MUSCLE STIMULATION SYSTEM",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K120511",
    "decision_date": "2012-07-30",
    "decision_code": "SESE",
    "applicant": "Leto Enterprise , Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K120511",
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  },
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    "brand": "Carol Cole Company",
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    "device_name": "TRINITY WRINKLE REMOVER",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K120560",
    "decision_date": "2012-11-06",
    "decision_code": "SESE",
    "applicant": "Carol Cole Company",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K120560",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
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  },
  {
    "brand": "Led Intellectual Properties, LLC",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LIGHT FOR WRINKLES",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K120775",
    "decision_date": "2012-06-04",
    "decision_code": "SESE",
    "applicant": "Led Intellectual Properties, LLC",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K120775",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Home Skinovations , Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "SILKN BLUE",
    "product_code": "OLP",
    "category": "acne-light",
    "k_number": "K121435",
    "decision_date": "2013-02-22",
    "decision_code": "SESE",
    "applicant": "Home Skinovations , Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K121435",
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    "brand": "La Lumiere, LLC",
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    "applicant": "La Lumiere, LLC",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K123999",
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    "brand": "Syneron Beauty",
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    "applicant": "Syneron Beauty",
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    "brand": "Espansione Marketing S.P.A",
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    "applicant": "Biosonic Technologies, LLC",
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    "brand": "Silverbay, LLC, D/B/A Quasar Bio-Tech",
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    "brand": "Carol Cole Company",
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  },
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    "brand": "Led Intellectual Properties, LLC",
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    "applicant": "Led Intellectual Properties, LLC",
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    "brand": "Home Skinovations , Ltd.",
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    "brand": "Wellquest Intl., Inc.",
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    "brand": "Biorenew Labs, LLC",
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    "brand": "Accord Media",
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    "applicant": "Accord Media",
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    "brand": "Nutra Luxe MD, LLC",
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    "brand": "Cynosure, Inc.",
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    "brand": "Ps Advanced Engineering",
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    "brand": "Carol Cole Company",
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    "brand": "Trophy Skin, Inc.",
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    "applicant": "Trophy Skin, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K133896",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
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    "brand": "El Global Trade, Ltd.",
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    "category": "ipl-laser-hair",
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    "applicant": "El Global Trade, Ltd.",
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    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
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    "brand": "La Lumiere, LLC",
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    "k_number": "K140471",
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    "applicant": "La Lumiere, LLC",
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    "brand": "Led Technologies, LLC",
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    "brand": "Home Skinovations , Ltd.",
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    "brand": "Nutra Luxe MD, LLC",
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    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
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    "brand": "Led Intellectual Properties, LLC",
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    "brand": "Everyway Medical Instruments Co.,Ltd",
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    "brand": "Wuhan Lotuxs Technology Co., Ltd.",
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    "brand": "Ipulse Limited",
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    "brand": "Centre Light Solutions, LLC",
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    "brand": "Omm Imports Inc Dba Zero Gravity",
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    "brand": "Michael Todd, LP",
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    "brand": "Zuko, Inc.",
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    "brand": "Foreo, Inc.",
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    "brand": "Zhongshan Bisen Plastic Electronic Products Co., Ltd.",
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    "brand": "Li-Tek Electronic Technology Corporation",
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    "brand": "Home Skinovations , Ltd.",
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    "brand": "Dermal Photonics Corporation",
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    "brand": "Liaoning Sidey Optoelectronics Technologies Co., Ltd.",
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    "category": "ipl-laser-hair",
    "k_number": "K163173",
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    "brand": "Pulsaderm, LLC",
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    "brand": "Shenzhen Siken 3D Technology Development Co., Ltd.",
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    "brand": "Habalan Med & Beauty Co.,Ltd",
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    "applicant": "Habalan Med & Beauty Co.,Ltd",
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    "brand": "Cyden Limited",
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    "device_name": "iPulse SmoothSkin BARE Hair Removal Device",
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    "applicant": "Cyden Limited",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K163552",
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    "brand": "Pulsaderm, LLC",
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    "brand": "Oriental Inspiration Limited",
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    "device_name": "Hee HR Mini",
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    "applicant": "Oriental Inspiration Limited",
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    "brand": "El Global Trade, Ltd.",
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    "brand": "Lg Electronics",
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    "brand": "Biophotas, Inc.",
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    "brand": "Led Technologies, Inc.",
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    "applicant": "Led Technologies, Inc.",
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    "brand": "Home Skinovations , Ltd.",
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    "brand": "Carol Cole Company Dba Nuface",
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    "brand": "Infinitus (China) Company , Ltd.",
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    "applicant": "Infinitus (China) Company , Ltd.",
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    "brand": "Heat IN A Click",
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    "brand": "El Global Trade, Ltd.",
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    "brand": "Omm Imports, Inc. D/B/A Zero Gravity",
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    "brand": "Conair Corporation",
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    "brand": "Shenzhen Mareal Tech Co., Ltd.",
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    "brand": "Omm Imports D/B/A Zero Gravity",
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    "brand": "Tama Research Corporation",
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    "applicant": "Tama Research Corporation",
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    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
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  },
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    "brand": "Shen Zhen Cosbeauty Co., Ltd.",
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    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
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    "brand": "Shenzhen Mismon Technology Co., Ltd.",
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    "brand": "Led Technologies, Inc.",
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    "brand": "Shenzhen Gsd Tech Co., Ltd.",
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    "category": "ipl-laser-hair",
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    "brand": "Led Technologies, Inc.",
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    "brand": "Led Technologies, Inc.",
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    "applicant": "Led Technologies, Inc.",
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    "brand": "Johnson & Johnson Consumer, Inc.",
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    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K180847",
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    "brand": "Medtek Skincare, LLC",
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    "brand": "Uvbiotek, LLC",
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    "brand": "Micro Current Technology, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Ultra Facial Toning System",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K181062",
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    "applicant": "Micro Current Technology, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K181062",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Home Well Trading, Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Beurer IPL 5500 device/ IPL 5000/ IPL PureSkin Pro",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K181121",
    "decision_date": "2018-06-28",
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    "applicant": "Home Well Trading, Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K181121",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Medical Device Branch of Zhangzhou Easepal Industrial Co.,Lt",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Salon Hair Reduction System",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K181568",
    "decision_date": "2018-09-11",
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    "applicant": "Medical Device Branch of Zhangzhou Easepal Industrial Co.,Lt",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K181568",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Premier North America, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Avologi ENEO",
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    "category": "led",
    "k_number": "K181659",
    "decision_date": "2018-07-26",
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    "applicant": "Premier North America, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K181659",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Home Well Trading, Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Beurer IPL 8500 device/ IPL VelvetSkin Pro",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K181734",
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    "decision_code": "SESE",
    "applicant": "Home Well Trading, Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K181734",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Carol Cole Company Dba Nuface",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "NuFACE FIX Skin Toning Device",
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    "category": "microcurrent",
    "k_number": "K182424",
    "decision_date": "2018-12-18",
    "decision_code": "SESE",
    "applicant": "Carol Cole Company Dba Nuface",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K182424",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Pollogen, Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "STOP U (Packed Black USA), STOP U (Packed White USA)",
    "product_code": "PAY",
    "category": "rf",
    "k_number": "K182774",
    "decision_date": "2019-06-19",
    "decision_code": "SESE",
    "applicant": "Pollogen, Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K182774",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22PAY%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Led Technologies, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "dpl SpotLite",
    "product_code": "OLP",
    "category": "acne-light",
    "k_number": "K183118",
    "decision_date": "2019-02-07",
    "decision_code": "SESE",
    "applicant": "Led Technologies, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K183118",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OLP%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Micro Current Technology, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Ultra OTC Facial Toning System",
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    "k_number": "K183189",
    "decision_date": "2019-04-17",
    "decision_code": "SESE",
    "applicant": "Micro Current Technology, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K183189",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Touchbeauty Beauty & Health (Shenzhen) Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K183217",
    "decision_date": "2019-02-15",
    "decision_code": "SESE",
    "applicant": "Touchbeauty Beauty & Health (Shenzhen) Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K183217",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
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  },
  {
    "brand": "Led Technologies, Inc.",
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    "device_name": "dpl Faceware",
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    "category": "led",
    "k_number": "K183247",
    "decision_date": "2019-03-14",
    "decision_code": "SESE",
    "applicant": "Led Technologies, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K183247",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "El Global Trade, Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Sensilight Pro / Pistol IPL",
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    "category": "ipl-laser-hair",
    "k_number": "K183260",
    "decision_date": "2019-03-18",
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    "applicant": "El Global Trade, Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K183260",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
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  },
  {
    "brand": "Lg Electronics.Inc",
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    "device_name": "LG PRA.L DERMA LED MASK",
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    "category": "led",
    "k_number": "K183671",
    "decision_date": "2019-01-22",
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    "applicant": "Lg Electronics.Inc",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K183671",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
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  },
  {
    "brand": "Medtek Skincare, LLC",
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    "device_name": "Poly Clear",
    "product_code": "OLP",
    "category": "acne-light",
    "k_number": "K183708",
    "decision_date": "2019-09-17",
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    "applicant": "Medtek Skincare, LLC",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K183708",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OLP%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
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    "brand": "Xtreem Pulse, LLC",
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    "k_number": "K190269",
    "decision_date": "2019-08-28",
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    "applicant": "Xtreem Pulse, LLC",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K190269",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
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    "brand": "Cyden Limited",
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    "device_name": "BRAUN Silk.expert Pro 5",
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    "category": "ipl-laser-hair",
    "k_number": "K190354",
    "decision_date": "2019-03-18",
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    "applicant": "Cyden Limited",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K190354",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
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    "brand": "Cyden Limited",
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    "device_name": "BRAUN Silk Expert Pro 3",
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    "category": "ipl-laser-hair",
    "k_number": "K190366",
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    "applicant": "Cyden Limited",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K190366",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
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    "brand": "Galactic Beauty, LLC",
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    "device_name": "MMSphere",
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    "k_number": "K190443",
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    "applicant": "Galactic Beauty, LLC",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K190443",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
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  },
  {
    "brand": "Kam Yuen Plastic Products , Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Aimanfun Lumea Comfort",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K190820",
    "decision_date": "2019-10-02",
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    "applicant": "Kam Yuen Plastic Products , Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K190820",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Ismart Marketing Svcs, Ltd.",
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    "device_name": "faceLITE",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K191629",
    "decision_date": "2019-09-12",
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    "applicant": "Ismart Marketing Svcs, Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K191629",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
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    "brand": "Carol Cole Company Dba Nuface",
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    "k_number": "K191672",
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    "applicant": "Carol Cole Company Dba Nuface",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K191672",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
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    "brand": "Avazzia, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Avazzia OTC TENS for aesthetics, model BEST-AV1\u0099: EZZI-LIFT\u0099 Device",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K191951",
    "decision_date": "2021-04-27",
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    "applicant": "Avazzia, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K191951",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
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    "brand": "Cyden Limited",
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    "device_name": "SmoothSkin BARE+",
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    "category": "ipl-laser-hair",
    "k_number": "K192010",
    "decision_date": "2019-09-24",
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    "applicant": "Cyden Limited",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K192010",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
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    "brand": "Vupiesse S.R.L",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Tua Face Fitness / Tua Trend Face",
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    "k_number": "K192077",
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    "applicant": "Vupiesse S.R.L",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K192077",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Beijing Adss Development Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "PDT-FACE",
    "product_code": "OLP",
    "category": "acne-light",
    "k_number": "K192295",
    "decision_date": "2020-05-01",
    "decision_code": "SESE",
    "applicant": "Beijing Adss Development Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K192295",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OLP%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Bosidin Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Home Use Hair Removal Device Model(s): D-1128, D-1103, D-1119, D-1129, D-1130",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K192432",
    "decision_date": "2019-11-08",
    "decision_code": "SESE",
    "applicant": "Shenzhen Bosidin Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K192432",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
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    "brand": "Cyden Limited",
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    "device_name": "SmoothSkin Pure",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K200184",
    "decision_date": "2020-02-21",
    "decision_code": "SESE",
    "applicant": "Cyden Limited",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K200184",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Foreo, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "BEAR and BEAR mini",
    "product_code": "NFO",
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    "k_number": "K200803",
    "decision_date": "2020-07-31",
    "decision_code": "SESE",
    "applicant": "Foreo, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K200803",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Ningbo Hesi Electric Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Infrared light therapy led facial light therapy mask-Derma plus, Photons Facial Skin Care Machine LED Beauty Mask Therapy Beauty Machine",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K200983",
    "decision_date": "2021-07-14",
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    "applicant": "Ningbo Hesi Electric Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K200983",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Gtg Wellness Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Opera Lebody (Gold), Opera Lebody (Zafiro)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K201107",
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    "decision_code": "SESE",
    "applicant": "Gtg Wellness Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K201107",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Carole Cole Company",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "NuFACE Mini Plus",
    "product_code": "NFO",
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    "k_number": "K201680",
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    "decision_code": "SESE",
    "applicant": "Carole Cole Company",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K201680",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Carol Cole Company Dba Nuface",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "NuFace Trinity Plus Device",
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    "k_number": "K201782",
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    "decision_code": "SESE",
    "applicant": "Carol Cole Company Dba Nuface",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K201782",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Carol Cole Company Dba Nuface",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Trinity ELE Plus and Trinity ELE Plus Pro",
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    "k_number": "K201906",
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    "applicant": "Carol Cole Company Dba Nuface",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K201906",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Heat IN A Click, LLC",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Looper (Model: ZX-579S)",
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    "category": "acne-light",
    "k_number": "K202055",
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    "applicant": "Heat IN A Click, LLC",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K202055",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OLP%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Kaiyan Medical CO , Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Aduro Light Beauty Mask",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K202390",
    "decision_date": "2021-07-14",
    "decision_code": "SESE",
    "applicant": "Shenzhen Kaiyan Medical CO , Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K202390",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Carewear Corp.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Carewear Firefly Wrinkle Reduction",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K202442",
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    "applicant": "Carewear Corp.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K202442",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Kaiyan Medical CO , Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "DemarkQ WOW, DemarkQ POP",
    "product_code": "OLP",
    "category": "acne-light",
    "k_number": "K203214",
    "decision_date": "2021-07-22",
    "decision_code": "SESE",
    "applicant": "Shenzhen Kaiyan Medical CO , Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K203214",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OLP%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Kaiyan Medical CO , Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Aduro light therapy Handheld",
    "product_code": "OLP",
    "category": "acne-light",
    "k_number": "K203271",
    "decision_date": "2021-07-21",
    "decision_code": "SESE",
    "applicant": "Shenzhen Kaiyan Medical CO , Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K203271",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OLP%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Weikai Technology Co.,Ltd",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair removal",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K203510",
    "decision_date": "2021-02-26",
    "decision_code": "SESE",
    "applicant": "Shenzhen Weikai Technology Co.,Ltd",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K203510",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Pollogen, Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "STOP U Model UXV Device",
    "product_code": "PAY",
    "category": "rf",
    "k_number": "K203665",
    "decision_date": "2021-02-25",
    "decision_code": "SESE",
    "applicant": "Pollogen, Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K203665",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22PAY%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Mismon Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Home Use IPL Beauty Device, Model(s): MS-208B, MS-212B, MS-216B, MS-218B, MELSYA-M6, MELSYA-M7.",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K210311",
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    "decision_code": "SESE",
    "applicant": "Shenzhen Mismon Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K210311",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Guangzhou Haoxingwan Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Superior Hair Remover",
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    "category": "ipl-laser-hair",
    "k_number": "K210376",
    "decision_date": "2021-10-07",
    "decision_code": "SESE",
    "applicant": "Guangzhou Haoxingwan Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K210376",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Marci Beauty, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Infrared Red blue LED light heat beauty machine, Infrared Red blue LED light heat beauty machine, Infrared Red blue LED light heat beauty machine",
    "product_code": "OLP",
    "category": "acne-light",
    "k_number": "K210545",
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    "decision_code": "SESE",
    "applicant": "Marci Beauty, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K210545",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OLP%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Lyma Life , Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LYMA Laser",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K210823",
    "decision_date": "2022-03-18",
    "decision_code": "SESE",
    "applicant": "Lyma Life , Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K210823",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Globalmed Technologies",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Omnilux CLEAR",
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    "category": "acne-light",
    "k_number": "K210948",
    "decision_date": "2021-06-24",
    "decision_code": "SESE",
    "applicant": "Globalmed Technologies",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K210948",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OLP%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Yrs Group, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Synergy",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K210954",
    "decision_date": "2021-06-29",
    "decision_code": "SESE",
    "applicant": "Yrs Group, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K210954",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Led Technologies, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "reVive Light Therapy Essentials",
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    "category": "led",
    "k_number": "K210965",
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    "applicant": "Led Technologies, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K210965",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Led Technologies, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "reVive Light Therapy Essentials",
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    "category": "acne-light",
    "k_number": "K210968",
    "decision_date": "2021-12-21",
    "decision_code": "SESE",
    "applicant": "Led Technologies, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K210968",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OLP%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen DJ Medical Equipment Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Microcurrent device (Model: HBR2-1)",
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    "category": "microcurrent",
    "k_number": "K211055",
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    "applicant": "Shenzhen DJ Medical Equipment Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K211055",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Qiaochengli Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal",
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    "category": "ipl-laser-hair",
    "k_number": "K211174",
    "decision_date": "2021-09-01",
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    "applicant": "Shenzhen Qiaochengli Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K211174",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Beauty Every Moment Intelligent Electric Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Home Use Hair Removal Device",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K211185",
    "decision_date": "2021-12-20",
    "decision_code": "SESE",
    "applicant": "Shenzhen Beauty Every Moment Intelligent Electric Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K211185",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Beauty Every Moment Intelligent Electric Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Home Use Hair Removal Device",
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    "category": "ipl-laser-hair",
    "k_number": "K211922",
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    "applicant": "Shenzhen Beauty Every Moment Intelligent Electric Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K211922",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Cyden Limited",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Braun Silk.expert Mini",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K211994",
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    "decision_code": "SESE",
    "applicant": "Cyden Limited",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K211994",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Theragun, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "TheraFace LED",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K212155",
    "decision_date": "2021-12-21",
    "decision_code": "SESE",
    "applicant": "Theragun, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K212155",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Theragun, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "TheraFace Microcurrent",
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    "k_number": "K212238",
    "decision_date": "2021-09-29",
    "decision_code": "SESE",
    "applicant": "Theragun, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K212238",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Aesthetic Technology, Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
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    "category": "led",
    "k_number": "K212275",
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    "applicant": "Aesthetic Technology, Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K212275",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Zhongshan Bisen Plastic Electronic Products Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K212314",
    "decision_date": "2021-10-21",
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    "applicant": "Zhongshan Bisen Plastic Electronic Products Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K212314",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Dongguan Define Beauty Electronic Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K212318",
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    "applicant": "Dongguan Define Beauty Electronic Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K212318",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Ziip, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "ZIIP+ Device",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K212342",
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    "decision_code": "SESE",
    "applicant": "Ziip, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K212342",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Leaflife Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Leaf Smooth",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K212697",
    "decision_date": "2021-11-19",
    "decision_code": "SESE",
    "applicant": "Shenzhen Leaflife Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K212697",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Led Intellectual Properties, LLC",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LightStim Elipsa",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K212771",
    "decision_date": "2022-01-26",
    "decision_code": "SESE",
    "applicant": "Led Intellectual Properties, LLC",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K212771",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Fansizhe Science and Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Intense Pulsed Light (IPL) System",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K212881",
    "decision_date": "2022-04-11",
    "decision_code": "SESE",
    "applicant": "Shenzhen Fansizhe Science and Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K212881",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Century Dongyuan Technology CO , Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device, model: AI01",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K212897",
    "decision_date": "2021-11-04",
    "decision_code": "SESE",
    "applicant": "Shenzhen Century Dongyuan Technology CO , Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K212897",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Carol Cole Company Dba Nuface",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Trinity Plus Wrinkle Reducer",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K212947",
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    "decision_code": "SESE",
    "applicant": "Carol Cole Company Dba Nuface",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K212947",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Borria Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL hair removal machine",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K213020",
    "decision_date": "2021-12-16",
    "decision_code": "SESE",
    "applicant": "Shenzhen Borria Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K213020",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Kaiyan Medical CO , Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Oren LED Perioral Light Therapy System",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K213024",
    "decision_date": "2021-12-22",
    "decision_code": "SESE",
    "applicant": "Shenzhen Kaiyan Medical CO , Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K213024",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Li-Tek Electronics Technology C0., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Micro-current facial cold and hot service (model: TPML-100)",
    "product_code": "OLP",
    "category": "acne-light",
    "k_number": "K213039",
    "decision_date": "2022-05-25",
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    "applicant": "Li-Tek Electronics Technology C0., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K213039",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OLP%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Glan Electronics Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal, Model: OBT-02",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K213041",
    "decision_date": "2021-11-18",
    "decision_code": "SESE",
    "applicant": "Glan Electronics Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K213041",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Osto Technology Company Limited",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Facial Mask",
    "product_code": "OLP",
    "category": "acne-light",
    "k_number": "K213056",
    "decision_date": "2022-07-07",
    "decision_code": "SESE",
    "applicant": "Shenzhen Osto Technology Company Limited",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K213056",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OLP%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Johari Digital Healthcare Limited",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Myolift QT",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K213078",
    "decision_date": "2023-04-27",
    "decision_code": "SESE",
    "applicant": "Johari Digital Healthcare Limited",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K213078",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Mz Skin",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "MZ Skin LightMAX Supercharged LED Mask 2.0",
    "product_code": "OLP",
    "category": "acne-light",
    "k_number": "K213184",
    "decision_date": "2021-11-23",
    "decision_code": "SESE",
    "applicant": "Mz Skin",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K213184",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OLP%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Y & J Bio Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "easy Claire",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K213285",
    "decision_date": "2022-03-03",
    "decision_code": "SESE",
    "applicant": "Y & J Bio Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K213285",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Cyden Limited",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "SmoothSkin Pure Mini",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K213692",
    "decision_date": "2022-01-26",
    "decision_code": "SESE",
    "applicant": "Cyden Limited",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K213692",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Iluminage Beauty Co., Limited",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Home use hair removal device, model: Precise Touch Pro",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K213830",
    "decision_date": "2022-02-01",
    "decision_code": "SESE",
    "applicant": "Iluminage Beauty Co., Limited",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K213830",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Premier North America, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "ENEO TOTALE (Model: ENEOT947)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K213841",
    "decision_date": "2022-01-06",
    "decision_code": "SESE",
    "applicant": "Premier North America, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K213841",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Premier North America, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Luminice",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K214100",
    "decision_date": "2022-02-24",
    "decision_code": "SESE",
    "applicant": "Premier North America, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K214100",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Duplex International Trading Limited",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Project E Beauty LED Light Therapy Mask (Model: PE730)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K214101",
    "decision_date": "2022-03-23",
    "decision_code": "SESE",
    "applicant": "Duplex International Trading Limited",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K214101",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Harpar Grace International",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Shani Darden LED light therapy mask",
    "product_code": "OLP",
    "category": "acne-light",
    "k_number": "K214103",
    "decision_date": "2022-03-22",
    "decision_code": "SESE",
    "applicant": "Harpar Grace International",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K214103",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OLP%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Qianyu Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Hand-held IPL device(JOVS Graphene Hair Removal Device)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K214113",
    "decision_date": "2022-03-28",
    "decision_code": "SESE",
    "applicant": "Shenzhen Qianyu Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K214113",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Yrs Group, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Synergy Marble (Model: Opasm)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K220064",
    "decision_date": "2022-07-22",
    "decision_code": "SESE",
    "applicant": "Yrs Group, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K220064",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Kaiyan Medical CO , Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Skin Care Beauty Mask (Model: MJ-06)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K220168",
    "decision_date": "2022-05-17",
    "decision_code": "SESE",
    "applicant": "Shenzhen Kaiyan Medical CO , Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K220168",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Ya-Man, Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Medi Lift PLUS",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K220198",
    "decision_date": "2023-06-28",
    "decision_code": "SESE",
    "applicant": "Ya-Man, Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K220198",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Yuwei Electronic Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device,  model(s): S1-A, S2-A, S1, S2, S3, S4",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K220222",
    "decision_date": "2022-04-26",
    "decision_code": "SESE",
    "applicant": "Shenzhen Yuwei Electronic Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K220222",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Mareal Tech Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Home use hair removal device",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K220248",
    "decision_date": "2022-07-01",
    "decision_code": "SESE",
    "applicant": "Shenzhen Mareal Tech Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K220248",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Pollogen, Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Pollogen STOP U Model UXV Device",
    "product_code": "PAY",
    "category": "rf",
    "k_number": "K220322",
    "decision_date": "2023-05-04",
    "decision_code": "SESE",
    "applicant": "Pollogen, Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K220322",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22PAY%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Qianyu Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Hand-held IPL device (JOVS Hair Removal Device)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K220645",
    "decision_date": "2022-04-27",
    "decision_code": "SESE",
    "applicant": "Shenzhen Qianyu Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K220645",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Junbobeauty Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL HAIR REMOVAL HANDSET, Model: IPL-666",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K220669",
    "decision_date": "2022-05-16",
    "decision_code": "SESE",
    "applicant": "Shenzhen Junbobeauty Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K220669",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Luminance Medical Ventures, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "The Luminance RED Acne Device",
    "product_code": "OLP",
    "category": "acne-light",
    "k_number": "K220729",
    "decision_date": "2022-06-09",
    "decision_code": "SESE",
    "applicant": "Luminance Medical Ventures, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K220729",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OLP%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Qiaochengli Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K220927",
    "decision_date": "2022-06-02",
    "decision_code": "SESE",
    "applicant": "Shenzhen Qiaochengli Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K220927",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Beauty Every Moment Intelligent Electric Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Home Use Hair Removal Device",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K221001",
    "decision_date": "2022-05-12",
    "decision_code": "SESE",
    "applicant": "Shenzhen Beauty Every Moment Intelligent Electric Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K221001",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device, Model(s): UI04A, UI04B, UI04C",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K221002",
    "decision_date": "2022-06-01",
    "decision_code": "SESE",
    "applicant": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K221002",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Hunan Guangye Biotechnology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Beauty LED Mask, Model: KFB265",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K221151",
    "decision_date": "2022-07-19",
    "decision_code": "SESE",
    "applicant": "Hunan Guangye Biotechnology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K221151",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Semlamp Intelligent Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal (Model: SL-B080, SL-B126, SL-B136)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K221246",
    "decision_date": "2022-07-07",
    "decision_code": "SESE",
    "applicant": "Shenzhen Semlamp Intelligent Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K221246",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Led Technologies, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "reVive Light Therapy LED Cleansing System",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K221430",
    "decision_date": "2022-07-27",
    "decision_code": "SESE",
    "applicant": "Led Technologies, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K221430",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Xtreem Pulse, LLC",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "PureLift Pro Plus",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K221443",
    "decision_date": "2022-10-21",
    "decision_code": "SESE",
    "applicant": "Xtreem Pulse, LLC",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K221443",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Light Tree Ventures Europe B.V.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Eye Perfector, model: EY-36A, EY-36B",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K221444",
    "decision_date": "2022-12-08",
    "decision_code": "SESE",
    "applicant": "Light Tree Ventures Europe B.V.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K221444",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Lizbella Technology Co.,Ltd",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL hair removal",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K221451",
    "decision_date": "2022-08-01",
    "decision_code": "SESE",
    "applicant": "Shenzhen Lizbella Technology Co.,Ltd",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K221451",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Century Dongyuan Technology CO , Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device, model: AI01, AI06, AI08, AI16, AI17",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K221466",
    "decision_date": "2022-08-12",
    "decision_code": "SESE",
    "applicant": "Shenzhen Century Dongyuan Technology CO , Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K221466",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Ulike Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Diamond Air+ (UI04A, UI04B, UI04C)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K221553",
    "decision_date": "2022-09-15",
    "decision_code": "SESE",
    "applicant": "Ulike Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K221553",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Fansizhe Science and Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Intense Pulsed Light (IPL) System, model: T013C, T015C, T015K",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K221569",
    "decision_date": "2022-06-30",
    "decision_code": "SESE",
    "applicant": "Shenzhen Fansizhe Science and Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K221569",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Desida Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL sapphire ice cooling hair remove device",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K221635",
    "decision_date": "2022-08-31",
    "decision_code": "SESE",
    "applicant": "Shenzhen Desida Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K221635",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Desida Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Hair Removal Device (Model: IPL-D26, IPL-D19)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K221643",
    "decision_date": "2022-10-21",
    "decision_code": "SESE",
    "applicant": "Shenzhen Desida Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K221643",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Mywin Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Remover, Model: G993, G996, G998 and G885",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K221679",
    "decision_date": "2022-07-07",
    "decision_code": "SESE",
    "applicant": "Shenzhen Mywin Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K221679",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Light Tree Ventures Europe B.V.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Light Therapy Mask (model: MK-78, MK-04, MK66-H, MK66R-B, EL00003)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K221775",
    "decision_date": "2022-12-20",
    "decision_code": "SESE",
    "applicant": "Light Tree Ventures Europe B.V.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K221775",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Light Tree Ventures Europe B.V.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Light Therapy Mask (model: MK66R-B)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K221946",
    "decision_date": "2022-11-22",
    "decision_code": "SESE",
    "applicant": "Light Tree Ventures Europe B.V.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K221946",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Foreo, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "FAQ 101",
    "product_code": "PAY",
    "category": "rf",
    "k_number": "K222012",
    "decision_date": "2023-04-05",
    "decision_code": "SESE",
    "applicant": "Foreo, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K222012",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22PAY%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Goodwind Technology Development Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K222316",
    "decision_date": "2022-09-28",
    "decision_code": "SESE",
    "applicant": "Shenzhen Goodwind Technology Development Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K222316",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Cellreturn Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Led Mask Platinum Md",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K222377",
    "decision_date": "2022-11-03",
    "decision_code": "SESE",
    "applicant": "Cellreturn Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K222377",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Hunan Guangye Biotechnology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device, Model(s): KCA423,  KCA437, KCA439",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K222432",
    "decision_date": "2022-10-11",
    "decision_code": "SESE",
    "applicant": "Hunan Guangye Biotechnology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K222432",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Ishine Technology Company Limited",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device, Model(s): skn001,skn005,skn006,skn002,RoseSkinCo Lumi",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K222537",
    "decision_date": "2022-10-14",
    "decision_code": "SESE",
    "applicant": "Shenzhen Ishine Technology Company Limited",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K222537",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Noble Smart Manufacturing Tech Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K222598",
    "decision_date": "2022-11-17",
    "decision_code": "SESE",
    "applicant": "Shenzhen Noble Smart Manufacturing Tech Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K222598",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Dermal Photonics Corp",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "NIRA Model 2",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K222685",
    "decision_date": "2023-02-08",
    "decision_code": "SESE",
    "applicant": "Dermal Photonics Corp",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K222685",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Siken 3D Technology Development Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Cooling Hair Removal Device",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K222710",
    "decision_date": "2022-12-01",
    "decision_code": "SESE",
    "applicant": "Shenzhen Siken 3D Technology Development Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K222710",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Myblend",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "myLEDmask",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K223147",
    "decision_date": "2023-05-14",
    "decision_code": "SESE",
    "applicant": "Myblend",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K223147",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Y & J Bio Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "easy Claire",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K223278",
    "decision_date": "2022-11-17",
    "decision_code": "SESE",
    "applicant": "Y & J Bio Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K223278",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Led Technologies, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "reVive Light Therapy\u00ae Wrinkle and Acne LED Device",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K223482",
    "decision_date": "2022-12-21",
    "decision_code": "SESE",
    "applicant": "Led Technologies, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K223482",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Morlaser Shenzhen Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal, Model(s): SB01, SB01A, SB01B, SB01C, SN02, SN03",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K223524",
    "decision_date": "2023-02-16",
    "decision_code": "SESE",
    "applicant": "Morlaser Shenzhen Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K223524",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Guangdong Newdermo Biotech Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED light therapy mask (FM-01, FM-02, FM-03)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K223544",
    "decision_date": "2023-02-23",
    "decision_code": "SESE",
    "applicant": "Guangdong Newdermo Biotech Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K223544",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device, Model(s): UI06 PN, UI06 PL, UI06 JL, UI06 BR, UI06 DB, UI06 PR, UI06 OG, UI06 RD",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K223618",
    "decision_date": "2023-02-28",
    "decision_code": "SESE",
    "applicant": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K223618",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Light Tree Ventures Europe B.V.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Infrared Heat (Model: E0221)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K223893",
    "decision_date": "2023-05-16",
    "decision_code": "SESE",
    "applicant": "Light Tree Ventures Europe B.V.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K223893",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Bemer Int AG",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "B.Light Clear Evo and B.Light Restore Evo",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K223919",
    "decision_date": "2023-09-23",
    "decision_code": "SESE",
    "applicant": "Bemer Int AG",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K223919",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Fansizhe Science and Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Intense Pulsed Light (IPL) System, model: T023K, T023A, T023B, T023C, T023D, T023E, T021K, T021A, T001A, T001B, T001M, T001N, T011C, T016K",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K223928",
    "decision_date": "2023-03-28",
    "decision_code": "SESE",
    "applicant": "Shenzhen Fansizhe Science and Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K223928",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Silk'N Beauty , Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Silk'n Titan Allways",
    "product_code": "PAY",
    "category": "rf",
    "k_number": "K230013",
    "decision_date": "2023-08-30",
    "decision_code": "SESE",
    "applicant": "Silk'N Beauty , Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K230013",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22PAY%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Yangyi Technology ., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device, Model(s): AP10, AP20, AP30, AP32",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K230021",
    "decision_date": "2023-03-31",
    "decision_code": "SESE",
    "applicant": "Shenzhen Yangyi Technology ., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K230021",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Ivylaser (Beijing) Technology Co.,Ltd",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IVYLASER Handhold Hair Removal Machine",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K230025",
    "decision_date": "2023-07-03",
    "decision_code": "SESE",
    "applicant": "Ivylaser (Beijing) Technology Co.,Ltd",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K230025",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Light Tree Ventures Europe B.V.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Q-Rejuvalight Pro Facewear (Model: P19-0023)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K230042",
    "decision_date": "2023-04-28",
    "decision_code": "SESE",
    "applicant": "Light Tree Ventures Europe B.V.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K230042",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Gsd Tech Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Light Based Hair Removal Device GP592",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K230060",
    "decision_date": "2023-03-03",
    "decision_code": "SESE",
    "applicant": "Shenzhen Gsd Tech Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K230060",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Wuhan Lotuxs Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Diode Laser Hair Removal",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K230090",
    "decision_date": "2023-04-19",
    "decision_code": "SESE",
    "applicant": "Wuhan Lotuxs Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K230090",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Bsx Technology Electronics Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device, Model(s): BSXT101, BSXT102, BSXT103, BSXT105, BSXT106, BSXT108",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K230097",
    "decision_date": "2023-04-06",
    "decision_code": "SESE",
    "applicant": "Shenzhen Bsx Technology Electronics Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K230097",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Kam Yuen Plastic Products , Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Aimanfun Lumea Comfort, Model: A-2788, A-2789 and A-3588",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K230107",
    "decision_date": "2023-04-05",
    "decision_code": "SESE",
    "applicant": "Kam Yuen Plastic Products , Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K230107",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device, Model(s): UI04\u00a0SD, UI04\u00a0DG",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K230122",
    "decision_date": "2023-04-10",
    "decision_code": "SESE",
    "applicant": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K230122",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Light Tree Ventures Europe B.V.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LUSTRE ClearSkin Renew Pro Facewear Mask(Model: PR4001)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K230124",
    "decision_date": "2023-03-15",
    "decision_code": "SESE",
    "applicant": "Light Tree Ventures Europe B.V.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K230124",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Therabody, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "TheraFace Mask",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K230293",
    "decision_date": "2023-06-09",
    "decision_code": "SESE",
    "applicant": "Therabody, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K230293",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Sungpo Hi-Tech Electronic Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Facial Mask",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K230351",
    "decision_date": "2023-05-05",
    "decision_code": "SESE",
    "applicant": "Shenzhen Sungpo Hi-Tech Electronic Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K230351",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Jizhimei Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Cooling Hair Removal Device, Model(s): NBB01, NBB02",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K230360",
    "decision_date": "2023-04-10",
    "decision_code": "SESE",
    "applicant": "Shenzhen Jizhimei Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K230360",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Leaflife Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Planar LED mate",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K230362",
    "decision_date": "2023-09-11",
    "decision_code": "SESE",
    "applicant": "Shenzhen Leaflife Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K230362",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "21 Equipment S.R.L.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "C.C. Life 21",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K230459",
    "decision_date": "2023-10-19",
    "decision_code": "SESE",
    "applicant": "21 Equipment S.R.L.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K230459",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Miley Technology (Hebei) Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device Models: MLY-T069",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K230473",
    "decision_date": "2023-06-15",
    "decision_code": "SESE",
    "applicant": "Miley Technology (Hebei) Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K230473",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Dongguan Hunter Electronic Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "PMD Clean Acne, Model: 4004-CABLUE-NA, 4004-GREY-NA, 4004-YELLOW-NA, 4004-PSTO-NA, 4004-LPUR-NA, 4004-CABLUE-NA-INT, 4004-GREY-INT, 4004-YELLOW-INT, 4004-PSTO-INT, 4004-LPUR-INT",
    "product_code": "OLP",
    "category": "acne-light",
    "k_number": "K230490",
    "decision_date": "2023-10-27",
    "decision_code": "SESE",
    "applicant": "Dongguan Hunter Electronic Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K230490",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OLP%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Xtreem Pulse",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "PureLift Pro Edition",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K230506",
    "decision_date": "2023-06-21",
    "decision_code": "SESE",
    "applicant": "Xtreem Pulse",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K230506",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Xiazhifeng Electronic Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device, Model(s): FY-B505AL, FY-B505AG, FY-B505BL, FY-B505BG, FY-B507AL, FY-B507AG, FY-B507BL, FY-B507BG, FY-B508AL, FY-B508AG, FY-B508BL, FY-B508BG, FY-B509AL, FY-B509AG, FY-B509BL, FY-B509BG",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K230549",
    "decision_date": "2023-04-25",
    "decision_code": "SESE",
    "applicant": "Shenzhen Xiazhifeng Electronic Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K230549",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Light Tree Ventures Europe B.V.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LUSTRE 3XPRESS Light Beauty Therapy patches, model: PR6001, PR5001",
    "product_code": "OLP",
    "category": "acne-light",
    "k_number": "K230720",
    "decision_date": "2023-07-03",
    "decision_code": "SESE",
    "applicant": "Light Tree Ventures Europe B.V.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K230720",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OLP%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Ionka Medical Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Hand-held IPL device (IPL Home Use Hair Removal Device), Model: FZ-608, FZ-608G, FZ-100, FZ-200",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K230739",
    "decision_date": "2023-05-26",
    "decision_code": "SESE",
    "applicant": "Shenzhen Ionka Medical Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K230739",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Cyden Limited",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Braun Skin i.expert",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K230911",
    "decision_date": "2023-04-27",
    "decision_code": "SESE",
    "applicant": "Cyden Limited",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K230911",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Zhongshan Qizhe Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device Model: Skin Expert Pro IPL 008, Skin Expert Pro IPL 008S",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K231215",
    "decision_date": "2023-06-26",
    "decision_code": "SESE",
    "applicant": "Zhongshan Qizhe Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K231215",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "iSMART Developments, Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LUMA LED patches (LUMA Blemish (TN2197) and LUMA Revive (TN2189))",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K231555",
    "decision_date": "2023-07-27",
    "decision_code": "SESE",
    "applicant": "iSMART Developments, Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K231555",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Zhuzhou Goldenhot Medical Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Intense pulsed light device, Model(s): DE01A-B, DE01A-G, DE01B-B, DE01B-G, DE01C-B, DE01C-G, DE02A-B, DE02A-G, DE02B-B, DE02B-G, DE02C-B, DE02C-G.",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K231613",
    "decision_date": "2023-07-31",
    "decision_code": "SESE",
    "applicant": "Zhuzhou Goldenhot Medical Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K231613",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Foshan Jindi Electric Appliance Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Home Use Hair Removal Device, Model(s): JD-TM002, JD-TM003, JD-TM012, JD-TM016, JD-TM022",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K231717",
    "decision_date": "2023-09-06",
    "decision_code": "SESE",
    "applicant": "Foshan Jindi Electric Appliance Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K231717",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Qianyu Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device, Model(s): JP1, JR3, JR8, JR9",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K231800",
    "decision_date": "2023-09-07",
    "decision_code": "SESE",
    "applicant": "Shenzhen Qianyu Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K231800",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Foreo, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "PEACH 2, PEACH 2 Duo, PEACH 2 go",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K231977",
    "decision_date": "2023-09-25",
    "decision_code": "SESE",
    "applicant": "Foreo, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K231977",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Nse Products, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Nu Skin RenuSpa iO",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K232001",
    "decision_date": "2023-11-21",
    "decision_code": "SESE",
    "applicant": "Nse Products, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K232001",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Dongguan Lide Electric Appliance Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device, Model(s): PB1, PB2, PB3, PB4, TM002",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K232056",
    "decision_date": "2023-10-06",
    "decision_code": "SESE",
    "applicant": "Dongguan Lide Electric Appliance Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K232056",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Wochuan Electronic Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal, Model: W-1095, W-1098",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K232124",
    "decision_date": "2023-09-14",
    "decision_code": "SESE",
    "applicant": "Shenzhen Wochuan Electronic Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K232124",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "BTL Industries, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "BTL-785BNF Handpiece",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K232172",
    "decision_date": "2023-09-18",
    "decision_code": "SESE",
    "applicant": "BTL Industries, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K232172",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Koli Technology Co.,Ltd",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device, Model(s): T1, T2, T3, T7, T10",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K232183",
    "decision_date": "2023-09-22",
    "decision_code": "SESE",
    "applicant": "Shenzhen Koli Technology Co.,Ltd",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K232183",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Foreo, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "BEAR 2 Body",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K232242",
    "decision_date": "2024-05-13",
    "decision_code": "SESE",
    "applicant": "Foreo, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K232242",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Lumenessa Corp",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL hair removal device",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K232274",
    "decision_date": "2023-09-28",
    "decision_code": "SESE",
    "applicant": "Lumenessa Corp",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K232274",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "El Global Trade, Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "CurrentBody Skin RF",
    "product_code": "PAY",
    "category": "rf",
    "k_number": "K232424",
    "decision_date": "2024-03-06",
    "decision_code": "SESE",
    "applicant": "El Global Trade, Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K232424",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22PAY%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Lescolton Electrical Appliance Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device (LS-T106, LS-T107, LS-T108)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K232499",
    "decision_date": "2023-10-11",
    "decision_code": "SESE",
    "applicant": "Shenzhen Lescolton Electrical Appliance Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K232499",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Jianchao Intelligent Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Hair Removal Device, Model(s): R2815-G Pro, R2815-G",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K232575",
    "decision_date": "2023-11-20",
    "decision_code": "SESE",
    "applicant": "Shenzhen Jianchao Intelligent Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K232575",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Premier North America, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "BLU TOTALE (Model: ENEOB852)",
    "product_code": "OLP",
    "category": "acne-light",
    "k_number": "K232656",
    "decision_date": "2023-11-14",
    "decision_code": "SESE",
    "applicant": "Premier North America, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K232656",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OLP%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Stg24 Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Led Mask Platinum Exclusive MD",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K232795",
    "decision_date": "2023-12-07",
    "decision_code": "SESE",
    "applicant": "Stg24 Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K232795",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Siken 3D Technology Development Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Cooling Hair Removal Device",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K232845",
    "decision_date": "2023-11-14",
    "decision_code": "SESE",
    "applicant": "Shenzhen Siken 3D Technology Development Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K232845",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Meik Beauty Industry Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Light Based Hair Removal Device",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K232846",
    "decision_date": "2023-12-07",
    "decision_code": "SESE",
    "applicant": "Shenzhen Meik Beauty Industry Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K232846",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Radiant Renewal Skincare Wand (HD-15, HD-15A)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K232863",
    "decision_date": "2023-12-13",
    "decision_code": "SESE",
    "applicant": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K232863",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Greatro Electronic Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Intense Pulse Light Therapeutic Apparatus",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K232932",
    "decision_date": "2023-12-04",
    "decision_code": "SESE",
    "applicant": "Shenzhen Greatro Electronic Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K232932",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Borria Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K232939",
    "decision_date": "2023-12-15",
    "decision_code": "SESE",
    "applicant": "Shenzhen Borria Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K232939",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Belega, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Beagank 4T Plus",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K233010",
    "decision_date": "2023-11-21",
    "decision_code": "SESE",
    "applicant": "Belega, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K233010",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Idea Light Limited",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED silicone mask (Model: LP-RVTGLWP-WHT, LP-RVTGLW-WHT, TLM200)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K233114",
    "decision_date": "2024-01-12",
    "decision_code": "SESE",
    "applicant": "Shenzhen Idea Light Limited",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K233114",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Micro Current Technology, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "MF SC Facial Toning System",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K233525",
    "decision_date": "2023-11-24",
    "decision_code": "SESE",
    "applicant": "Micro Current Technology, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K233525",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Eye mask (EY-20R, A20, EY-20N)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K233556",
    "decision_date": "2024-01-04",
    "decision_code": "SESE",
    "applicant": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K233556",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device (UI06 PN, UI06 PL, UI06 JL, UI06 BR, UI06 DB, UI06 PR, UI06 OG, UI06 RD,UI06 WH, UI06 MG, UI06 OB, UI06 LY,UI06 IG,)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K233664",
    "decision_date": "2024-01-11",
    "decision_code": "SESE",
    "applicant": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K233664",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Body Trim Industrial Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Facial Toning device (UIC-189); Facial Toning device (UIC-589)",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K233667",
    "decision_date": "2024-02-12",
    "decision_code": "SESE",
    "applicant": "Body Trim Industrial Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K233667",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device (UI04 MK,UI04 BN,UI04 BU,UI04 CB,UI04 GY,UI04 LG,UI04 DG,UI04 PL,UI04 PN,UI04 SD,UI04 SG,UI04 MG)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K233679",
    "decision_date": "2024-01-05",
    "decision_code": "SESE",
    "applicant": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K233679",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Pollogen, Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Geneo X Elite",
    "product_code": "PAY",
    "category": "rf",
    "k_number": "K233766",
    "decision_date": "2024-05-07",
    "decision_code": "SESE",
    "applicant": "Pollogen, Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K233766",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22PAY%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Cyden Limited",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "SmoothSkin Pure Adapt (SSG3)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K233782",
    "decision_date": "2023-12-20",
    "decision_code": "SESE",
    "applicant": "Cyden Limited",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K233782",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Premier North America, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "NUNA LUX (NUNL528)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K233862",
    "decision_date": "2024-03-01",
    "decision_code": "SESE",
    "applicant": "Premier North America, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K233862",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device (UI06PN, UI06 PL, UI06 JL, UI06 BR, UI06 DB, UI06 PR, UI06 OG, UI06 RD, UI08 BR, UI08 DB, UI08 BL, UI08 GP, UI08 PN, UI08 RE, UI08 WH, UI08 PW, UI07 BR, UI07 DB, UI07 BL, UI07 GP, UI07 PN, UI07 RE, UI07 WH, UI07 PW, UI20 BR, UI20 DB, UI20 BL, UI20 GP, UI20 PN, UI20 RE, UI20 WH, UI20 PW)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K233887",
    "decision_date": "2024-01-22",
    "decision_code": "SESE",
    "applicant": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K233887",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Jianrong Biomedical Electronics Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device (YT01,YT02,YT03,YT04)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K240016",
    "decision_date": "2024-07-10",
    "decision_code": "SESE",
    "applicant": "Shenzhen Jianrong Biomedical Electronics Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K240016",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Face Patches (MT-12MA, MT-12MC)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K240089",
    "decision_date": "2024-04-10",
    "decision_code": "SESE",
    "applicant": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K240089",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Shuge Medical Beauty Devices Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Home Use Hair Removal Device (SJ15)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K240093",
    "decision_date": "2024-04-24",
    "decision_code": "SESE",
    "applicant": "Shenzhen Shuge Medical Beauty Devices Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K240093",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen\u00a0Mlay\u00a0Intelligent\u00a0Technology\u00a0Co.,\u00a0, Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Home Use Hair Removal Device (Model(s):T10A, T10B, T10C, T10D, T11A, T15A, T17A, T18A, T14A, T16A, T19A)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K240264",
    "decision_date": "2024-03-08",
    "decision_code": "SESE",
    "applicant": "Shenzhen\u00a0Mlay\u00a0Intelligent\u00a0Technology\u00a0Co.,\u00a0, Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K240264",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Dongguan Boyuan Intelligent Technology Co.,Ltd",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device (model: KCA450, KCA446, KCA504, KCA505, KCA506, KCA507, KCA508, KCA509, KCA501, KCA423, KCA448, KCA449, KCA502, KCA521)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K240282",
    "decision_date": "2024-04-03",
    "decision_code": "SESE",
    "applicant": "Dongguan Boyuan Intelligent Technology Co.,Ltd",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K240282",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Qianyu Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Wrinkle Treatment Device (JM2)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K240360",
    "decision_date": "2024-04-05",
    "decision_code": "SESE",
    "applicant": "Shenzhen Qianyu Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K240360",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Foreo, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "FAQ\u0099 201, FAQ\u0099 202",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K240378",
    "decision_date": "2024-04-19",
    "decision_code": "SESE",
    "applicant": "Foreo, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K240378",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Carol Cole Company Dba Nuface\u00ae",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "NuFACE\u00ae FIX+",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K240564",
    "decision_date": "2024-06-27",
    "decision_code": "SESE",
    "applicant": "Carol Cole Company Dba Nuface\u00ae",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K240564",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Beauty Every Moment Intelligent Electric Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Home Use Hair Removal Device (D-1199, D-T099, D-T018, D-T019, D-T003B, D-T003W, D-T018Y, D-T019Y, D-1196B, D-1196W, D-1196C, D-1196C1, D-T099K, D-T099KW, D-T012, D-T012W)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K240583",
    "decision_date": "2024-06-18",
    "decision_code": "SESE",
    "applicant": "Shenzhen Beauty Every Moment Intelligent Electric Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K240583",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Cyden Limited",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "SmoothSkin Pure Unplugged (SSB3)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K240587",
    "decision_date": "2024-03-29",
    "decision_code": "SESE",
    "applicant": "Cyden Limited",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K240587",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Foreo, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "FAQ\u0099 (102)",
    "product_code": "PAY",
    "category": "rf",
    "k_number": "K240616",
    "decision_date": "2024-07-15",
    "decision_code": "SESE",
    "applicant": "Foreo, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K240616",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22PAY%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Ice Cooling IPL Hair Removal Device (UI07 BR, UI07 DB, UI07 BL, UI07 GP, UI07 PN, UI07 RE, UI07 WH, UI07 PW, UI20 BR, UI20 DB, UI20 BL, UI20GP, UI20 PN, UI20 RE, UI20 WH, UI20 PW)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K240649",
    "decision_date": "2024-06-21",
    "decision_code": "SESE",
    "applicant": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K240649",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Ice Cooling IPL Hair Removal Device (UI06 PN, UI06 PL, UI06 JL, UI06 BR, UI06 DB, UI06 PR, UI06 OG,UI06 RD,UI06 WH, UI06 MG, UI06 OB, UI06 LY, UI06 IG, UIM20 GR, UIM20 BK, UIM20 SL, UIM20 CB, UIM20 WR)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K240652",
    "decision_date": "2024-04-04",
    "decision_code": "SESE",
    "applicant": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K240652",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Semlamp Intelligent Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal (SL-B287, SL-B329, SL-B301-1, SL-B328)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K240969",
    "decision_date": "2024-05-31",
    "decision_code": "SESE",
    "applicant": "Shenzhen Semlamp Intelligent Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K240969",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Foreo, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Luna 4 plus",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K241102",
    "decision_date": "2024-08-20",
    "decision_code": "SESE",
    "applicant": "Foreo, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K241102",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen\u00a0Mlay\u00a0Intelligent\u00a0Technology\u00a0Co.,\u00a0, Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Ice Cooling IPL Home Use Hair Removal Device (Model(s): T10B, T10C, T15A, T17A, T18A, T14A, T16A, T19A)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K241106",
    "decision_date": "2024-05-22",
    "decision_code": "SESE",
    "applicant": "Shenzhen\u00a0Mlay\u00a0Intelligent\u00a0Technology\u00a0Co.,\u00a0, Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K241106",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Qiaocheng LI (Dongguan) Medical Instruments Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Intense pulsed light therapy apparatus (FDA01, FDA02, FDA03, FDA04S, FDA05S, FDA06, FDA06S, FDA07, FDA07S, FDA08, FDA09S, FDA10S)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K241120",
    "decision_date": "2024-06-24",
    "decision_code": "SESE",
    "applicant": "Qiaocheng LI (Dongguan) Medical Instruments Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K241120",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Dongguan Hunter Electronic Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "PMD Clean Redvolution (4005-moab-NA, 4005-moab-INT, 4005-pepper-NA, 4005-pepper-INT, 4005-cream-NA, 4005-cream-INT, 4005-twilight-NA , 4005-twilight-INT, 4005-grey-NA, 4005-grey- INT)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K241203",
    "decision_date": "2024-07-25",
    "decision_code": "SESE",
    "applicant": "Dongguan Hunter Electronic Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K241203",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Ice Cooling IPL Hair Removal Device (Y6S GR, Y6S GA,Y6S GT, Y6S JU, Y6S JM, Y6S MU, Y6S OG, Y6S CH,Y6S PN,Y6S NK, Y6S PG, Y6S TG, Y6S OE)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K241205",
    "decision_date": "2024-09-09",
    "decision_code": "SESE",
    "applicant": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K241205",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Lescolton Electrical Appliance Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device (LS-T121, LS-T121A, LS-T121B, LS-T121C, LS-T130, LS-T130A, LST130B, LS-T133, LS-T135, LS-T136, LS-T137, LS-T134, LS-T138, LS-T139, LS-T140)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K241343",
    "decision_date": "2024-07-09",
    "decision_code": "SESE",
    "applicant": "Shenzhen Lescolton Electrical Appliance Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K241343",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Aozemei Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Micro-current Facial Beauty Device (AM-810B, AM-810W, AM-812B, AM-812W)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K241718",
    "decision_date": "2024-10-28",
    "decision_code": "SESE",
    "applicant": "Shenzhen Aozemei Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K241718",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Yang WO Electronic Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device (BE932C, BE932D, BE932E)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K241834",
    "decision_date": "2024-09-23",
    "decision_code": "SESE",
    "applicant": "Shenzhen Yang WO Electronic Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K241834",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Dongguan Boyuan Intelligent Technology Co.,Ltd",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Light Therapy Device (KFB290, KFB291, KFB265, KFB293)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K241857",
    "decision_date": "2024-10-11",
    "decision_code": "SESE",
    "applicant": "Dongguan Boyuan Intelligent Technology Co.,Ltd",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K241857",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Junmei Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device (JM-843, JM-865, JM-638)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K241881",
    "decision_date": "2024-08-29",
    "decision_code": "SESE",
    "applicant": "Shenzhen Junmei Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K241881",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "HIGHERDOSE Red and Infrared Light Mask (MK66-L)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K241933",
    "decision_date": "2024-09-27",
    "decision_code": "SESE",
    "applicant": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K241933",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "EnergyLounger (TY-01)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K241947",
    "decision_date": "2025-03-03",
    "decision_code": "SESE",
    "applicant": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K241947",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Ice Cooling IPL Hair Removal Device (UI20 DB, UI20 RE, UI20 GP, UI20 PW, UI20S DB, UI20S RE, UI20S PW, UI20S GP,UI20 WH, UI20 GR, UI20 BS, UI20 MP, UI20 BL, UI20 PN, UI20 BR, UI20WG, UI20S WH, UI20S GR, UI20S BS, UI20S MP)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K241998",
    "decision_date": "2024-12-13",
    "decision_code": "SESE",
    "applicant": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K241998",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Ice Cooling IPL Hair Removal Device (UIM20 GR, UIM20 BK, UIM20 SL, UIM20 CB, UIM20 WR)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K242039",
    "decision_date": "2024-11-06",
    "decision_code": "SESE",
    "applicant": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K242039",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Ningbo Dechang Electrical Machinery Made Co.,Ltd",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Light Therapy Mask (RT01)",
    "product_code": "OLP",
    "category": "acne-light",
    "k_number": "K242068",
    "decision_date": "2025-04-04",
    "decision_code": "SESE",
    "applicant": "Ningbo Dechang Electrical Machinery Made Co.,Ltd",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K242068",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OLP%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Nuon Medical Equipment Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Radiant Renewal Skincare Wand (HD-44,HD-44A ,HD-44B,HD-44C, HD-69, HD-69A, HD-69B)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K242151",
    "decision_date": "2025-04-08",
    "decision_code": "SESE",
    "applicant": "Shenzhen Nuon Medical Equipment Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K242151",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Huaruibo Electric Appliances Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device (DH4, DH5, DH5 Plus, DH5 Max)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K242197",
    "decision_date": "2024-10-17",
    "decision_code": "SESE",
    "applicant": "Shenzhen Huaruibo Electric Appliances Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K242197",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Pollogen, Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "GENEO X ELITE",
    "product_code": "PAY",
    "category": "rf",
    "k_number": "K242227",
    "decision_date": "2025-10-12",
    "decision_code": "SESE",
    "applicant": "Pollogen, Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K242227",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22PAY%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "iSMART Developments, Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "d\u00e9coLITE LED Device",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K242382",
    "decision_date": "2024-11-08",
    "decision_code": "SESE",
    "applicant": "iSMART Developments, Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K242382",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Borria Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Therapy Mask (MN1, M226)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K242385",
    "decision_date": "2025-04-07",
    "decision_code": "SESE",
    "applicant": "Shenzhen Borria Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K242385",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "BTL Industries, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "BTL-785BNF-E",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K242532",
    "decision_date": "2024-12-13",
    "decision_code": "SESE",
    "applicant": "BTL Industries, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K242532",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "CurrentBody\u0099 LED 4 in 1 Zone Facial Mapping Mask (MK-90C, MK-90M, MK66RB-F, MK-90N)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K242593",
    "decision_date": "2025-02-14",
    "decision_code": "SESE",
    "applicant": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K242593",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Greatro Electronic Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Intense Pulse Light Therapeutic Apparatus (IPL-18 BF, IPL-18 FG)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K242595",
    "decision_date": "2024-11-07",
    "decision_code": "SESE",
    "applicant": "Shenzhen Greatro Electronic Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K242595",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Walton Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Light Therapy Machine (G1, G3, G4, G6)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K242638",
    "decision_date": "2024-11-27",
    "decision_code": "SESE",
    "applicant": "Shenzhen Walton Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K242638",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Nuon Medical Equipment Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-59C, HD-59D, HD-70, HD-72, HD-72A, HD-73A, HD-73B, HD-116, HD-116A, HD-53A, HD-53B)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K242700",
    "decision_date": "2024-12-19",
    "decision_code": "SESE",
    "applicant": "Shenzhen Nuon Medical Equipment Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K242700",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Jianchao Intelligent Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Hair Removal Device (R3C16-P, R3C16-W, R3C16-G, R3C16-P Pro, R3C16-W Pro, R3C16-G Pro, R3505-W, R3505-B, R3505-W Pro, R3505-B Pro)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K242710",
    "decision_date": "2024-12-06",
    "decision_code": "SESE",
    "applicant": "Shenzhen Jianchao Intelligent Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K242710",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Dongguan Laiguang Electronic Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Bestqool LED Therapy Device (LMK-001,LMK-004,LMK-005,LMK-006)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K242789",
    "decision_date": "2025-01-02",
    "decision_code": "SESE",
    "applicant": "Dongguan Laiguang Electronic Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K242789",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Sharkninja Operating, LLC",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "CryoGlow (FW3XXXX)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K242796",
    "decision_date": "2024-11-27",
    "decision_code": "SESE",
    "applicant": "Sharkninja Operating, LLC",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K242796",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Foshan Newface Electronic Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device (NV-TM10A, NV-TM10C, NV-TM10D)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K243017",
    "decision_date": "2025-05-06",
    "decision_code": "SESE",
    "applicant": "Foshan Newface Electronic Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K243017",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Ulike Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Diamond Air+ (UI04A, UI04B, UI04C, UI04M, UI04G, UI04W)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K243030",
    "decision_date": "2024-10-25",
    "decision_code": "SESE",
    "applicant": "Ulike Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K243030",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Bestway Plastic and Metal Products , Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device (BHRL-01, BHRL-02, BHRL-03, BHRL-04, BHRL-05, BHRL-06, BHRL-06B, BHRL-07, BHRL-08, BHRL-09, BHRL-10, BHRL-11, BHRL-12, BHRL-13, BHRL-14, BHRL-15, BHRL-16, BHRL-17, BHRL-18, BHRL-19, BHRL-20, BHRL-21, BHRL-22, BHRL-23, BHRL-24, BHRL-25, BHRL-26, BHRL-27, BHRL-28, BHRL-29)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K243036",
    "decision_date": "2025-06-15",
    "decision_code": "SESE",
    "applicant": "Bestway Plastic and Metal Products , Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K243036",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Siken 3D Technology Development Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Light Therapy Mask (SKB-1818P,SKB-1918,SKB-1918P,SKB-1918PLUS,SKB-2318L,SKB-2318P,SKB-2318PRO,IN-FM002, SKB-2418)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K243040",
    "decision_date": "2024-12-20",
    "decision_code": "SESE",
    "applicant": "Shenzhen Siken 3D Technology Development Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K243040",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Raja Trading Company, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Myolight Microcurrent Handpiece",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K243063",
    "decision_date": "2025-02-10",
    "decision_code": "SESE",
    "applicant": "Raja Trading Company, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K243063",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "EMA Aesthetics , Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Pr\u00e9ime DermaFacial  (MicroT)",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K243072",
    "decision_date": "2025-04-01",
    "decision_code": "SESE",
    "applicant": "EMA Aesthetics , Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K243072",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Zhuzhou Goldenhot Medical Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device (DE03A-W, DE03A-P, DE03A-V, DE03A-G, DE03B-W, DE03B-P, DE03B-V, DE03B-G)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K243085",
    "decision_date": "2024-12-21",
    "decision_code": "SESE",
    "applicant": "Zhuzhou Goldenhot Medical Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K243085",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Lyma Life , Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LYMA Laser PRO",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K243330",
    "decision_date": "2025-02-21",
    "decision_code": "SESE",
    "applicant": "Lyma Life , Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K243330",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Cyden Limited",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "SmoothSkin Pure Switch (SSC1)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K243362",
    "decision_date": "2024-11-27",
    "decision_code": "SESE",
    "applicant": "Cyden Limited",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K243362",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "JMOON NouvelleSkin Facial Toning Device (M30U PR, M30U MW, M30U SG, M30U SK, M30U MP)",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K243393",
    "decision_date": "2025-02-03",
    "decision_code": "SESE",
    "applicant": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K243393",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Rainbow Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Light Therapy Mask (Model(s): RB-008, RB-030, RB-081, RB-008G, RB-008GB, RB-008J, RB-008JB)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K243423",
    "decision_date": "2025-01-28",
    "decision_code": "SESE",
    "applicant": "Shenzhen Rainbow Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K243423",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Aozemei Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Micro-current Facial Beauty Device (AM-810B, AM-810W, AM-812B, AM-812W)",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K243430",
    "decision_date": "2024-12-19",
    "decision_code": "SESE",
    "applicant": "Shenzhen Aozemei Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K243430",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Philips Consumer Lifestyle B.V.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Philips Lumea IPL",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K243453",
    "decision_date": "2025-02-10",
    "decision_code": "SESE",
    "applicant": "Philips Consumer Lifestyle B.V.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K243453",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Ulike Reglow Light Therapy Device (UM10)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K243492",
    "decision_date": "2025-01-10",
    "decision_code": "SESE",
    "applicant": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K243492",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Eyco Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED light therapy mask (E43, E32, E49B, E49C, E100B, E100C, E103B, E104B, E106A, E108A)",
    "product_code": "OLP",
    "category": "acne-light",
    "k_number": "K243555",
    "decision_date": "2025-02-05",
    "decision_code": "SESE",
    "applicant": "Shenzhen Eyco Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K243555",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OLP%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Xtreem Pulse, LLC",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "PureLift GLOW",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K243587",
    "decision_date": "2025-03-06",
    "decision_code": "SESE",
    "applicant": "Xtreem Pulse, LLC",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K243587",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Sunsred Technology Co.,Ltd",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Facial Mask",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K243978",
    "decision_date": "2025-06-20",
    "decision_code": "SESE",
    "applicant": "Shenzhen Sunsred Technology Co.,Ltd",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K243978",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Dachi Communication Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Microcurrent Facial Device (CEC101, EE0101, EEI101)",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K244004",
    "decision_date": "2025-07-10",
    "decision_code": "SESE",
    "applicant": "Shenzhen Dachi Communication Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K244004",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Qianyu Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Wrinkle Treatment Device (JM1, JM2B)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K244020",
    "decision_date": "2025-05-01",
    "decision_code": "SESE",
    "applicant": "Shenzhen Qianyu Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K244020",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Ya-Man, Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Medi Lift Mask",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K244048",
    "decision_date": "2025-01-16",
    "decision_code": "SESE",
    "applicant": "Ya-Man, Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K244048",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Xplr , Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LMNT O2",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K250125",
    "decision_date": "2025-03-24",
    "decision_code": "SESE",
    "applicant": "Xplr , Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K250125",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Mustech Electronics Co., Limited",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device (M8011, M8012, M8013, M8015, M8021, M8022, M8023, M8025, M7011, M7012, M7021, M7023)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K250131",
    "decision_date": "2025-03-19",
    "decision_code": "SESE",
    "applicant": "Mustech Electronics Co., Limited",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K250131",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Yang WO Electronic Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device (BE965A, BE965B, BE965C)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K250171",
    "decision_date": "2025-03-19",
    "decision_code": "SESE",
    "applicant": "Shenzhen Yang WO Electronic Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K250171",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Ice Cooling IPL Hair Removal Device (UI06S PR, UI06S PN, UI06S WH)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K250194",
    "decision_date": "2025-03-26",
    "decision_code": "SESE",
    "applicant": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K250194",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Qianyu Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "JOVS Electric Stimulation Beauty Device (JE2)",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K250227",
    "decision_date": "2025-10-17",
    "decision_code": "SESE",
    "applicant": "Shenzhen Qianyu Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K250227",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Dongguan Boyuan Intelligent Technology Co.,Ltd",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device (KCA511/KCA516/KCA522)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K250253",
    "decision_date": "2025-05-06",
    "decision_code": "SESE",
    "applicant": "Dongguan Boyuan Intelligent Technology Co.,Ltd",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K250253",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "El Global Trade, Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Sensilift Pro (ST300XXYYZZZ)",
    "product_code": "PAY",
    "category": "rf",
    "k_number": "K250341",
    "decision_date": "2026-01-06",
    "decision_code": "SESE",
    "applicant": "El Global Trade, Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K250341",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22PAY%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Geske Beauty Tech GmbH",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "SmartAppGuidedTM MicroCurrent Face-Lift Pen  6 in 1",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K250361",
    "decision_date": "2025-05-23",
    "decision_code": "SESE",
    "applicant": "Geske Beauty Tech GmbH",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K250361",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "El Global Trade, Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL400",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K250384",
    "decision_date": "2025-05-23",
    "decision_code": "SESE",
    "applicant": "El Global Trade, Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K250384",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Perfect Idea Technology Limited",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Aglaia LED Beauty Device (BP-D2309)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K250413",
    "decision_date": "2025-03-18",
    "decision_code": "SESE",
    "applicant": "Shenzhen Perfect Idea Technology Limited",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K250413",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Solawave 2-in-1 Skincare Mini (Model: 61043)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K250532",
    "decision_date": "2025-05-22",
    "decision_code": "SESE",
    "applicant": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K250532",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "KALA Red Light Face Mask (KALA-01)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K250581",
    "decision_date": "2025-05-30",
    "decision_code": "SESE",
    "applicant": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K250581",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Ya-Man, Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Medi Lift Essential Eye Mask",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K250618",
    "decision_date": "2025-10-29",
    "decision_code": "SESE",
    "applicant": "Ya-Man, Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K250618",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "KALA Therapy Wand (Model: KALA-03)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K250761",
    "decision_date": "2025-07-11",
    "decision_code": "SESE",
    "applicant": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K250761",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Sungrow Led Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Light Therapy Mask (G15, G15P, G15K, G11P, G11, G10, G13, G14, G17, VISO, PRANA, Chin2Chest, BBL-FACEMASK)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K250830",
    "decision_date": "2025-06-09",
    "decision_code": "SESE",
    "applicant": "Shenzhen Sungrow Led Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K250830",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Foshan Guangyu Weilai Medical Equipment Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED LIGHT MASK (A093)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K250880",
    "decision_date": "2025-06-20",
    "decision_code": "SESE",
    "applicant": "Foshan Guangyu Weilai Medical Equipment Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K250880",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Ice Cooling IPL Hair Removal Device (MI01 LP, MI01 CB, MI01 GR, MI01 PP, MI01 RM, MI01 WG, MI01 WH, MI01 BK;UI04S PP, UI04S BU, UI04S WH, UI04S PN)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K250938",
    "decision_date": "2025-05-23",
    "decision_code": "SESE",
    "applicant": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K250938",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Ice Cooling IPL Hair Removal Device (UI20S DB, UI20S RE, UI20S PW, UI20S GP, UI20S GR, UI20S BK, UI20 DB, UI20 RE, UI20 PW, UI20 GP, UI20 GR, UI20 BK)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K250942",
    "decision_date": "2025-07-11",
    "decision_code": "SESE",
    "applicant": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K250942",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "CurrentBody Skin\u0099 LED Light Therapy Mask Series 2 (MK-90H)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K250966",
    "decision_date": "2025-06-25",
    "decision_code": "SESE",
    "applicant": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K250966",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Chuangtong Yigou Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Hand-held Hair Removal Device (FZ-200A, FZ-201, FZ-202, CT05, CT06, CT07, CT08, CT09)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K251000",
    "decision_date": "2025-06-30",
    "decision_code": "SESE",
    "applicant": "Shenzhen Chuangtong Yigou Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K251000",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "TRUDERMAL Pro (ZLD-390)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K251012",
    "decision_date": "2025-08-14",
    "decision_code": "SESE",
    "applicant": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K251012",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Nuon Medical Equipment Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Radiant Renewal Skincare Lid  (HD-59A, HD-59B, HD-70); Radiant Renewal Skincare Wand (HD-44)",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K251034",
    "decision_date": "2025-10-12",
    "decision_code": "SESE",
    "applicant": "Shenzhen Nuon Medical Equipment Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K251034",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Guangzhou Ahead Intelligent Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Light Therapy System (M500, L6)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K251042",
    "decision_date": "2025-06-06",
    "decision_code": "SESE",
    "applicant": "Guangzhou Ahead Intelligent Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K251042",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Fansizhe Science and Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Intense Pulsed Light (IPL) System (T033KQ, T033KD, T033KF, T033MQ, T033MD, T033MF, T055KQ, T055KD, T055KH, T002AQ, T002AD, T002AF, T002BQ, T002BD, T002BF, T050KQ, T050KD, T050KF)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K251173",
    "decision_date": "2025-07-14",
    "decision_code": "SESE",
    "applicant": "Shenzhen Fansizhe Science and Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K251173",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen\u00a0Mlay\u00a0Intelligent\u00a0Technology\u00a0Co.,\u00a0, Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device (Model(s): T14B, T16B, T19B, T15B, T17C, T18B, T21A, T21B, T21C, T21D, T22A, T22B, T25B, T25C)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K251176",
    "decision_date": "2025-08-14",
    "decision_code": "SESE",
    "applicant": "Shenzhen\u00a0Mlay\u00a0Intelligent\u00a0Technology\u00a0Co.,\u00a0, Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K251176",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Enmind Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device (IPL-001, IPL-002)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K251398",
    "decision_date": "2025-10-02",
    "decision_code": "SESE",
    "applicant": "Shenzhen Enmind Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K251398",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Fittop Health Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Light Therapy Mask (FCM902, FCM905, FCM906, FCM908, 11-001-RBMASK, FCM910)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K251588",
    "decision_date": "2025-08-21",
    "decision_code": "SESE",
    "applicant": "Shenzhen Fittop Health Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K251588",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "ShenB Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Sunny Plus (Sunny)",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K251649",
    "decision_date": "2025-09-18",
    "decision_code": "SESE",
    "applicant": "ShenB Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K251649",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Liyoutong Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Light Therapy Mask (M01, M02, M06, M07, M08, M09)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K251667",
    "decision_date": "2025-08-07",
    "decision_code": "SESE",
    "applicant": "Shenzhen Liyoutong Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K251667",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Huachuangtong Industrial Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device (HCT-1208/HCT-1208B/HCT-1208L)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K251707",
    "decision_date": "2025-08-01",
    "decision_code": "SESE",
    "applicant": "Shenzhen Huachuangtong Industrial Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K251707",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "KALA MINI 2.0 (KALA-04)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K251781",
    "decision_date": "2025-09-04",
    "decision_code": "SESE",
    "applicant": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K251781",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K251825",
    "decision_date": "2025-10-01",
    "decision_code": "SESE",
    "applicant": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K251825",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Erchonia Corporation",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Erchonia EVRL",
    "product_code": "OLP",
    "category": "acne-light",
    "k_number": "K251843",
    "decision_date": "2025-09-12",
    "decision_code": "SESE",
    "applicant": "Erchonia Corporation",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K251843",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OLP%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Heat IN A Click, LLC",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "FEATHER 01 02 03 04 (Model:01)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K251871",
    "decision_date": "2025-08-15",
    "decision_code": "SESE",
    "applicant": "Heat IN A Click, LLC",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K251871",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "A-1 Engineering",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "NeurotriS  (SX2500); NeurotriS (SX3800)",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K251909",
    "decision_date": "2025-09-03",
    "decision_code": "SESE",
    "applicant": "A-1 Engineering",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K251909",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Miley Technology (Hebei) Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device (MLY-M011); IPL Hair Removal Device (MLY-M012); IPL Hair Removal Device (MLY-M013); IPL Hair Removal Device (MLY-M015); IPL Hair Removal Device (MLY-T001); IPL Hair Removal Device (MLY-T002)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K251914",
    "decision_date": "2025-09-15",
    "decision_code": "SESE",
    "applicant": "Miley Technology (Hebei) Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K251914",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Ice Cooling IPL Hair Removal Device (UI06S PR, UI06S PN, UI06S WH, UI06S PRU, UI06S PNU, UI06S WHU)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K251984",
    "decision_date": "2025-07-24",
    "decision_code": "SESE",
    "applicant": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K251984",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Touchbeauty\u00a0Beauty\u00a0&\u00a0Health\u00a0(\u00a0Shenzhen\u00a0)\u00a0Co.,\u00a0Ltd",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "VITA\u00a0Multi-Function\u00a0Head\u00a0Brush (TB-2443F, TB-2442AF, TB-2343F, TB-2442F)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K252053",
    "decision_date": "2025-10-27",
    "decision_code": "SESE",
    "applicant": "Touchbeauty\u00a0Beauty\u00a0&\u00a0Health\u00a0(\u00a0Shenzhen\u00a0)\u00a0Co.,\u00a0Ltd",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K252053",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Merchsource, LLC",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Light Therapy Mask (1019055)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K252093",
    "decision_date": "2025-10-16",
    "decision_code": "SESE",
    "applicant": "Merchsource, LLC",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K252093",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Merchsource, LLC",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Light Therapy Decollete Mask (1019135)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K252096",
    "decision_date": "2025-10-01",
    "decision_code": "SESE",
    "applicant": "Merchsource, LLC",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K252096",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Siken 3D Technology Development Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Multi-functional Facial Beauty Device (SKB-1703,SKB-1803,SKB-1809, SKB-1909, SKB-2109,SKB-2129,SKB-2208PRO, SKB-2209)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K252142",
    "decision_date": "2025-12-05",
    "decision_code": "SESE",
    "applicant": "Shenzhen Siken 3D Technology Development Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K252142",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Siken 3D Technology Development Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Multi-functional Facial Beauty Device ( SKB-1703,SKB-1803,SKB-1909, SKB-2003 SKB-2109,SKB-2129,SKB-2208PRO, SKB-2209)",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K252146",
    "decision_date": "2025-12-23",
    "decision_code": "SESE",
    "applicant": "Shenzhen Siken 3D Technology Development Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K252146",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Aura Medical, LLC",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Aura Glide  (FC40)",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K252187",
    "decision_date": "2025-12-23",
    "decision_code": "SESE",
    "applicant": "Aura Medical, LLC",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K252187",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Dongguan Yanxi Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Light Therapy Mask (2311, 2344, 2457, 2458)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K252189",
    "decision_date": "2025-09-12",
    "decision_code": "SESE",
    "applicant": "Dongguan Yanxi Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K252189",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Foshan Jindi Electric Appliance Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Home Use Hair Removal Device (JD-TM016, JD-TM023, JD-TM027, JD-TM028, JD-TM032)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K252209",
    "decision_date": "2025-10-10",
    "decision_code": "SESE",
    "applicant": "Foshan Jindi Electric Appliance Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K252209",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Micro Current Technology, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "MF SC GEN2 Facial Toning System",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K252218",
    "decision_date": "2025-07-18",
    "decision_code": "SESE",
    "applicant": "Micro Current Technology, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K252218",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Qiaochengli Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Home Use Hair Removal Device (Models: FDA11, FDA12, FDA13, FDA14, FDA15, FDA16, FDA17, FDA18, FDA19, FDA20, FDA21S, FDA22S, FDA23S, FDA24S, FDA25, FDA26, FDA27, FDA28, FDA29S, FDA30S, FDA31S)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K252234",
    "decision_date": "2025-10-14",
    "decision_code": "SESE",
    "applicant": "Shenzhen Qiaochengli Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K252234",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Zhenxing Ruitong Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "MEGELIN LED Light Therapy Mask (JML1, JML1+JML2); MEGELIN LED Light Therapy Mask (JML3, JML3+JML4); MEGELIN LED Light Therapy Mask (JML5, JML5+JML7); MEGELIN LED Light Therapy Mask (JML6, JML6+JML8); MEGELIN LED Light Therapy Mask (JML9, JML9+JML10)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K252264",
    "decision_date": "2025-10-17",
    "decision_code": "SESE",
    "applicant": "Shenzhen Zhenxing Ruitong Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K252264",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "ORA Method LED Gua Sha (GS-04)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K252272",
    "decision_date": "2025-10-09",
    "decision_code": "SESE",
    "applicant": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K252272",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Atop Lighting Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Beauty Mask (RLBXX)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K252308",
    "decision_date": "2025-11-13",
    "decision_code": "SESE",
    "applicant": "Atop Lighting Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K252308",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Jianchao Intelligent Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Facial & Body Beauty Device (INIA-BD001, INIA-BD002, INIA-BD003, INIA-BD004, F2C15, F3222 Pro, F5516, F3606, F2210 Pro, F5808, INIA-ED001, INIA-ED002, INIA-BLD001, E1507)",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K252553",
    "decision_date": "2025-10-09",
    "decision_code": "SESE",
    "applicant": "Shenzhen Jianchao Intelligent Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K252553",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "HIGHERDOSE Body Sculptor (Model: GS-03)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K252603",
    "decision_date": "2026-01-28",
    "decision_code": "SESE",
    "applicant": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K252603",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Alovea Healthcare Co. , Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device (I6 S1, I6 D1, I6 M1)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K252618",
    "decision_date": "2025-11-14",
    "decision_code": "SESE",
    "applicant": "Alovea Healthcare Co. , Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K252618",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "El Global Trade, Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "DeepSkin (DEP100)",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K252621",
    "decision_date": "2026-05-08",
    "decision_code": "SESE",
    "applicant": "El Global Trade, Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K252621",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Dachi Communication Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Microcurrent Facial Device (CEC101, EEI101)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K252642",
    "decision_date": "2025-11-19",
    "decision_code": "SESE",
    "applicant": "Shenzhen Dachi Communication Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K252642",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Ice Cooling IPL Hair Removal Device (UI20S BK, UI20S BS, UI20S DB, UI20S GP, UI20S GR, UI20S MP, UI20S PW, UI20S RE, UI20S WH, UI20WG;UI20 BK, UI20 BL, UI20 BR, UI20 BS, UI20 DB, UI20 GP, UI20 GR, UI20 MP, UI20 PN, UI20 PW, UI20 RE, UI20 WH; UI06 PN, UI06 PL, UI06 JL, UI06 BR, UI06 DB,UI06 PR, UI06 OG,UI06RD,UI06 WH, UI06 MG, UI06 OB, UI06 LY, UI06 IG; UI06S PR, UI06S PN, UI06S WH, UI06S PRU, UI06S PNU, UI06S WHU; UI04 MK, UI04 BN, UI04 BU, UI04 CB, UI04 GY, UI04 LG, UI04 DG, UI04 PL,",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K252804",
    "decision_date": "2025-10-01",
    "decision_code": "SESE",
    "applicant": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K252804",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Goodwind Technology Development Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Wrinkle Retreat Pro Light Therapy Face Mask (Model: PH-m03)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K252983",
    "decision_date": "2025-12-17",
    "decision_code": "SESE",
    "applicant": "Shenzhen Goodwind Technology Development Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K252983",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Guangdong Ace-Tec Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Therapy Mask (SR11CM, SR11CM1, SR11CM2, SR11CM3, SR11CM4, SR11CM5, SR11CM6, SR11CM7, SR11CM8)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K252994",
    "decision_date": "2025-12-08",
    "decision_code": "SESE",
    "applicant": "Guangdong Ace-Tec Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K252994",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Gu'An Yeolight Smart Electronics Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device (SYL001AZ, SYL002AZ)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K253035",
    "decision_date": "2025-11-19",
    "decision_code": "SESE",
    "applicant": "Gu'An Yeolight Smart Electronics Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K253035",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Xinlong Precision Plastic Mold Products Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Light Therapy Mask (M19, M19-1, M19-2, M19-3, M19-5, M19-6)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K253054",
    "decision_date": "2025-12-19",
    "decision_code": "SESE",
    "applicant": "Shenzhen Xinlong Precision Plastic Mold Products Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K253054",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Sunglor Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Light Therapy Device (SG-FSM, SG-NK, SG-CT)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K253073",
    "decision_date": "2025-11-19",
    "decision_code": "SESE",
    "applicant": "Sunglor Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K253073",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Sunglor Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Light Therapy Device (Models: SG-FM, SG-FE)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K253086",
    "decision_date": "2025-12-19",
    "decision_code": "SESE",
    "applicant": "Sunglor Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K253086",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Dongguan Yijiaming Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Light Therapy Device (HLGMZ-3W-G1V1,HLGMZ-3W-G2V1,HLG-GJXJ-G1V1,HGMZ-2W-G1V1, HGMZ-2W-G2V1,MRD-GJXJ-G1V1.)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K253135",
    "decision_date": "2025-12-23",
    "decision_code": "SESE",
    "applicant": "Dongguan Yijiaming Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K253135",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Heat IN A Click, LLC",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Feather/numiere 05 06 07 (05)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K253279",
    "decision_date": "2025-12-24",
    "decision_code": "SESE",
    "applicant": "Heat IN A Click, LLC",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K253279",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Dongguan Lide Electric Appliance Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device (KA-10, KA-11, KA-11C, KA-11D, KA-18, KA-20, KA-21, KA-21C)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K253304",
    "decision_date": "2025-11-25",
    "decision_code": "SESE",
    "applicant": "Dongguan Lide Electric Appliance Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K253304",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Saidi Light Therapy Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Light Therapy Face Mask (FM60X, FM60X-B, FM60X-W, FM80-W, FM80, VAP1, FM100X, FM100X-B, FM100X-W)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K253400",
    "decision_date": "2025-12-24",
    "decision_code": "SESE",
    "applicant": "Shenzhen Saidi Light Therapy Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K253400",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Mlay Intelligent Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device (Models: T31A, T32A)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K253666",
    "decision_date": "2026-02-23",
    "decision_code": "SESE",
    "applicant": "Shenzhen Mlay Intelligent Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K253666",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Foreo, Inc.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "FAQ\u0099 (LED Panel); FAQ\u0099 (Dual LED Panel)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K253683",
    "decision_date": "2026-02-20",
    "decision_code": "SESE",
    "applicant": "Foreo, Inc.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K253683",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Rainbow Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Light Therapy Mask (RB-051, RB-061, RB-071, RB-052, RB-062, RB-072, RB-053, RB-063, RB-073)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K253712",
    "decision_date": "2026-01-23",
    "decision_code": "SESE",
    "applicant": "Shenzhen Rainbow Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K253712",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Philips Consumer Lifestyle B.V.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Philips Lumea IPL",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K253754",
    "decision_date": "2025-12-23",
    "decision_code": "SESE",
    "applicant": "Philips Consumer Lifestyle B.V.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K253754",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Jianchao Intelligent Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Facial & Body Beauty Device (model: INIA-BD001, INIA-BD002, INIA-BD003, INIA-BD004, F2C15, F3222 Pro, F5516, F3606, F2210 Pro, F5808, INIA-ED001, INIA-ED002, INIA-BLD001, E1507)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K253833",
    "decision_date": "2026-01-30",
    "decision_code": "SESE",
    "applicant": "Shenzhen Jianchao Intelligent Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K253833",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Hanhua Opto Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Therapy Light (COB1400, HP1800PRO)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K253874",
    "decision_date": "2026-03-03",
    "decision_code": "SESE",
    "applicant": "Shenzhen Hanhua Opto Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K253874",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LUSTRE GoGlow Advanced LED Patches (PR8001, PR9001)",
    "product_code": "OLP",
    "category": "acne-light",
    "k_number": "K253878",
    "decision_date": "2026-03-04",
    "decision_code": "SESE",
    "applicant": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K253878",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OLP%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Fansizhe Science and Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Intense Pulsed Light (IPL) System (Models: T033KQ, T033KD, T033KF, T033MQ, T033MD, T033MF, T055KQ, T055KD, T055KH, T505KQ, T505KH, T505KF, SL-B505WM)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K253881",
    "decision_date": "2025-12-29",
    "decision_code": "SESE",
    "applicant": "Shenzhen Fansizhe Science and Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K253881",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "FACEGYM Pro Device (HD-109)",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K253932",
    "decision_date": "2026-07-23",
    "decision_code": "SESE",
    "applicant": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K253932",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "SZ KKS Silicone&Electronic Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Light Therapy Silicone Face Mask (kks-225, kks-280, kks-281)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K254007",
    "decision_date": "2026-02-12",
    "decision_code": "SESE",
    "applicant": "SZ KKS Silicone&Electronic Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K254007",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Neck Beauty Mask (ZLD-66A,ZLD-90E,ZLD-130,ZLD-180H)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K254025",
    "decision_date": "2026-06-16",
    "decision_code": "SESE",
    "applicant": "Shenzhen Kaiyan Medical Equipment Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K254025",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Chuangtong Yigou Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Hair Removal Device (CT10, CT10 Pro, CT11, CT11 Pro, CT12, CT12 Pro, CTU05, CTU07, CTU09, CTU012, CTU015, CTU X, DT015 Pro, DT015, DT017 Pro, DT017, DT025 Pro, DT025)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K254047",
    "decision_date": "2026-03-11",
    "decision_code": "SESE",
    "applicant": "Shenzhen Chuangtong Yigou Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K254047",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Desida Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Light Therapy Mask (Models: T2, RLD10)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K254079",
    "decision_date": "2026-03-16",
    "decision_code": "SESE",
    "applicant": "Shenzhen Desida Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K254079",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "NOOANCE",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED FACIAL MASK (MJ-66DB, MK-99, MK-99A, MK-99M, MJ-66C)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K260150",
    "decision_date": "2026-04-22",
    "decision_code": "SESE",
    "applicant": "NOOANCE",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K260150",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Touchbeauty Beauty & Health (Shenzhen) Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "VITA\u00a0Multi-Function\u00a0Head\u00a0Brush (TB-2343F, TB-2442F)",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K260179",
    "decision_date": "2026-06-03",
    "decision_code": "SESE",
    "applicant": "Touchbeauty Beauty & Health (Shenzhen) Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K260179",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Guangdong Newdermo Biotech Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Light Therapy Masks (LumiLips FAC07NA)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K260202",
    "decision_date": "2026-03-23",
    "decision_code": "SESE",
    "applicant": "Guangdong Newdermo Biotech Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K260202",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Hironic Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "SYNERJET PRO (SP-1003); InPhiuse (SP-1003); WOWJET (SP-1003)",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K260387",
    "decision_date": "2026-08-31",
    "decision_code": "SESE",
    "applicant": "Hironic Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K260387",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Light Tree Ventures Europe B.V.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "myLEDmask 2 (MJ-144)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K260415",
    "decision_date": "2026-05-12",
    "decision_code": "SESE",
    "applicant": "Light Tree Ventures Europe B.V.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K260415",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Ulike Reglow Light Therapy Device (UM10)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K260511",
    "decision_date": "2026-03-16",
    "decision_code": "SESE",
    "applicant": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K260511",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Semlamp Intelligent Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal (SL-B301, SL-B300, SL-B330, SL-B330-1, SL-B287-1, SL-B371, SL-B371-2, SL-B371-1, SL-B352, SL-B352-1, SL-B352-2, SL-B330-F)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K260518",
    "decision_date": "2026-04-21",
    "decision_code": "SESE",
    "applicant": "Shenzhen Semlamp Intelligent Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K260518",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Xiazhifeng Electronic Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "IPL Hair Removal Device (FL-B505AG, FL-B505AP, FL-B505AM, FL-B507AG, FL-B507AP, FL-B507AM, FL-B508AG, FL-B508AP, FL-B508AM, FL-B509AG, FL-B509AP, FL-B509AM, FL-B510G, FL-B510P, FL-B510M, FL-B511G, FL-B511P, FL-B511M, FL-B512AG, FL-B512AP, FL-B512AM, FL-B513AG, FL-B513AP, FL-B513AM)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K260594",
    "decision_date": "2026-05-20",
    "decision_code": "SESE",
    "applicant": "Shenzhen Xiazhifeng Electronic Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K260594",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "iSMART Developments, Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "5 Wavelength LED Facemask (TN2508)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K260598",
    "decision_date": "2026-07-24",
    "decision_code": "SESE",
    "applicant": "iSMART Developments, Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K260598",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "The Beauty Tech Group, Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "CurrentBody Skin LED Multi Light Therapy Mask (MK-110D)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K260715",
    "decision_date": "2026-06-03",
    "decision_code": "SESE",
    "applicant": "The Beauty Tech Group, Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K260715",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Ice Cooling IPL Hair Removal Device (UI20S DB, UI20S RE, UI20S PW, UI20S GP, UI20S GR, UI20S BK)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K260742",
    "decision_date": "2026-05-05",
    "decision_code": "SESE",
    "applicant": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K260742",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Kam Yuen Plastic Products , Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Facial Beauty Device (Facial Mask LED Beauty Device A-901; Facial LED & EMS Beauty Device A-902; Facial Mask LED & EMS Beauty Device A-907)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K260767",
    "decision_date": "2026-08-31",
    "decision_code": "SESE",
    "applicant": "Kam Yuen Plastic Products , Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K260767",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Guangxi Ulike Medical Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Ulike Clear Zero (YC10 BU)",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K260895",
    "decision_date": "2026-05-28",
    "decision_code": "SESE",
    "applicant": "Guangxi Ulike Medical Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K260895",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Guangdong Newdermo Biotech Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Light Therapy Mask (K9C-TK, K9C-K, K9P-YK, K9P-K, FM-03BK, FM-09K)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K260946",
    "decision_date": "2026-06-18",
    "decision_code": "SESE",
    "applicant": "Guangdong Newdermo Biotech Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K260946",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Guangdong Newdermo Biotech Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Light Therapy Masks (LED Face Mask Pro FAC08NA, LED Chest Mask Pro FAC09NA)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K261052",
    "decision_date": "2026-06-29",
    "decision_code": "SESE",
    "applicant": "Guangdong Newdermo Biotech Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K261052",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Ice Cooling IPL Hair Removal Device (UI06S PR, UI06S PN, UI06S WH, UI06S PRU, UI06S PNU, UI06S WHU)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K261325",
    "decision_date": "2026-05-21",
    "decision_code": "SESE",
    "applicant": "Shenzhen Ulike Smart Electronics Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K261325",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Guangdong Newdermo Biotech Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Light Therapy Masks (LED Face Mask Pulse (FAC06NA))",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K261370",
    "decision_date": "2026-09-16",
    "decision_code": "SESE",
    "applicant": "Guangdong Newdermo Biotech Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K261370",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Dongguan Miqiang Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "XPREEN LED Light Therapy Masks (XPRE322, XPRE326, XPRE327, XPRE342, XPRE368, XPRE422, XPRE434, XPRE451, XPRE455, XPRE457, XPRE448, XPRE335, XPRE350, XPRE420, XPRE436, XPRE339, XPRE445)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K261407",
    "decision_date": "2026-07-15",
    "decision_code": "SESE",
    "applicant": "Dongguan Miqiang Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K261407",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Termosalud S.L.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Chromix",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K261473",
    "decision_date": "2026-07-01",
    "decision_code": "SESE",
    "applicant": "Termosalud S.L.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K261473",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Led Intellectual Properties, LLC",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LightStim for Wrinkles (1984); LightStim for Acne (2038)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K261482",
    "decision_date": "2026-07-31",
    "decision_code": "SESE",
    "applicant": "Led Intellectual Properties, LLC",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K261482",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Duplex International Trading Limited",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Light Therapy Masks (PE748, PE749, PE756)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K261496",
    "decision_date": "2026-08-04",
    "decision_code": "SESE",
    "applicant": "Duplex International Trading Limited",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K261496",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Chuangtong Yigou Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Light Therapy Mask (M01, M02, M03, M05, M06, M07, M08)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K261601",
    "decision_date": "2026-08-07",
    "decision_code": "SESE",
    "applicant": "Shenzhen Chuangtong Yigou Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K261601",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Goodwind Technology Development Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Eye Recovery Pro (PH-e03)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K261602",
    "decision_date": "2026-08-10",
    "decision_code": "SESE",
    "applicant": "Shenzhen Goodwind Technology Development Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K261602",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Jianchao Intelligent Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Hair Removal Device (R3C16-G Pro, R3C16-V Pro)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K261705",
    "decision_date": "2026-08-10",
    "decision_code": "SESE",
    "applicant": "Shenzhen Jianchao Intelligent Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K261705",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Shenzhen Qianyu Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "LED Light Therapy Mask (JML1, JML1+JML2); LED Light Therapy Mask (JML3, JML3+JML4); LED Light Therapy Mask (JML5, JML5+JML7); LED Light Therapy Mask (JML6, JML6+JML8); LED Light Therapy Mask ( JML9, JML9+JML10)",
    "product_code": "OHS",
    "category": "led",
    "k_number": "K261851",
    "decision_date": "2026-08-04",
    "decision_code": "SESE",
    "applicant": "Shenzhen Qianyu Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K261851",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHS%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "CyDen Limited",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Braun Aura 7 (6041)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K261975",
    "decision_date": "2026-09-30",
    "decision_code": "SESE",
    "applicant": "CyDen Limited",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K261975",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Cyden Limited",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Braun Aura 9 (6042)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K261977",
    "decision_date": "2026-09-25",
    "decision_code": "SESE",
    "applicant": "Cyden Limited",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K261977",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "ONE BEAUTY Technology Co., Ltd.",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "Sapphire Cooling IPL Hair Removal Device (Ice 2.0, Ice 2.1, Ice 2.2, Ice 2.0B, Ice 2.1B, Ice 2.2B)",
    "product_code": "OHT",
    "category": "ipl-laser-hair",
    "k_number": "K262524",
    "decision_date": "2026-09-18",
    "decision_code": "SESE",
    "applicant": "ONE BEAUTY Technology Co., Ltd.",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K262524",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22OHT%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  },
  {
    "brand": "Xtreem Pulse, LLC",
    "brand_method": "applicant fallback; not a verified retail brand",
    "device_name": "PureLift Pro Max",
    "product_code": "NFO",
    "category": "microcurrent",
    "k_number": "K262861",
    "decision_date": "2026-09-11",
    "decision_code": "SESE",
    "applicant": "Xtreem Pulse, LLC",
    "fda_url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K262861",
    "source_url": "https://api.fda.gov/device/510k.json?search=product_code%3A%22NFO%22&limit=1000&skip=0&sort=decision_date%3Adesc",
    "retrieved": "2026-10-20"
  }
]