510(k) K261625 · NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes
FAQ (FAQ 401);FAQ (FAQ 402)
| Applicant | Foreo, Inc., Las Vegas NV, US |
| Decision | Substantially Equivalent, Oct 26, 2026 |
| Received | May 15, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K261625
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.