FDA records / Microcurrent
Is ZIIP ZIIP+ FDA cleared?
Yes — the FDA record names ZIIP ZIIP+.
The model name is matched to the linked record below. Clearance is specific to the device and stated use; it is not a performance ranking.
“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
Follow the FDA record.
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.