ZIIP+

Discontinued — see ZIIP HALO.

FDA cleared · K212342

“Cleared” means the FDA found the device substantially equivalent to one already legally sold, for a stated use. It isn’t proof it works for you. What clearance means

What it’s cleared for

The ZIIP+ Device is intended for facial and neck stimulation and is indicated for over-the-counter cosmetic use.

From the FDA filing (K212342, page 4) — verbatim — not yet human-reviewed · retrieved 2026-10-19

Who should skip it

Skip it if you're pregnant, have epilepsy or seizures, or have a pacemaker or other implanted electronic device. Source: Today.com: at-home microcurrent facials (aesthetician Gina Marí)

The FDA record

Yes — the FDA record names ZIIP ZIIP+.

K212342 · View FDA record

Device name in the FDA record: ZIIP+ Device
Applicant: Ziip, Inc.
Decision date: 2021-09-23
Product code: NFO: Stimulator, Transcutaneous Electrical, Aesthetic Purposes
Evidence: FDA record names this model; retail model variants are not inferred. openFDA source; retrieved 2026-10-19.

Is ZIIP ZIIP+ FDA cleared?

Specifications

Maximum output current at 500Ω: 309 µA · From FDA filing — not yet human-reviewed · page 7 · retrieved 2026-10-19
Treatment areas (see source for restrictions): face, neck · Source — not yet human-reviewed · retrieved 2026-10-19
Cordless: Yes · Source — not yet human-reviewed · retrieved 2026-10-19
Warranty (years): 2 · Source — not yet human-reviewed · retrieved 2026-10-19
Return window (days; conditions apply): 30 · Source — not yet human-reviewed · retrieved 2026-10-19
Unopened, unused products only; other return-policy conditions apply.

Technical details appear only after we’ve checked and cited a source.

Price

Discontinued

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Where to buy

Discontinued — see ZIIP HALO.

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