Home › Device types › NFO
Stimulator, Transcutaneous Electrical, Aesthetic Purposes
FDA product code NFO · Class 2 · Neurology
138
Registered devices
37
Adverse events
2
Recalls
79
510(k) clearances
Devices with this code
PURELIFT — Xtreem Pulse LLCNuon — Shenzhen Nuon Medical Equipment Co., Ltd.BEAR 2 go — Foreo ABJohari Digital Healthcare Ltd. — SYRMA JOHARI MEDTECH LIMITEDZIIP Beauty — ZIIP, INC.Nu Skin Facial Spa — NSE PRODUCTS, INC.Luna 4 Plus — Foreo ABNuFACE — Nufacebt-sculpt GEN2 — MICRO CURRENT TECHNOLOGY, INC.BEAR 2 Body — Foreo ABBEAR 2 eyes & lips — Foreo ABNuon — Shenzhen Nuon Medical Equipment Co., Ltd.BEAR™ — Foreo ABNu Skin RenuSpa iO — NSE PRODUCTS, INC.BEAR™ mini — Foreo ABMicroCurrent Face-Lift Pen 6 in 1 — GESKE Beauty Tech GmbHSilk'n — Silkn Beauty Ltd.Johari Digital Healthcare Ltd. — SYRMA JOHARI MEDTECH LIMITEDSilk'n — Silkn Beauty Ltd.Everyway — EVERYWAY MEDICAL INSTRUMENTS CO., LTD.FaceMaster — FACEMASTER OF BEVERLY HILLS, INC.Nuon — Shenzhen Nuon Medical Equipment Co., Ltd.Lumina NRG — Heatinaclick LLCMicroCurrent Face-Lift Pen 6 in 1 — GESKE Beauty Tech GmbH
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2012-01-06 | Ion Genius, Inc. | Wires do not meet performance standards under 21 CFR 898 and have unprotected electrode configurations. Additionally, devices were sold/distributed without 510( |
| 2012-01-06 | Ion Genius, Inc. | Wires do not meet performance standards under 21 CFR 898 and have unprotected electrode configurations. Additionally, devices were sold/distributed without 510( |
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