FDA 510(k)

NuFACE Mini Device

K-Number: K191672 · 2019-10-15

Decision Date2019-10-15

Product CodeNFO

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

NuFACE Mini Device is a medical device manufactured by Carol Cole Company Dba Nuface. It received FDA 510(k) clearance on 2019-10-15 under approval number K191672. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NuFACE Mini Device?

NuFACE Mini Device is a medical device that received FDA 510(k) clearance on 2019-10-15. It is manufactured by Carol Cole Company Dba Nuface. The 510(k) number is K191672.

When was NuFACE Mini Device approved by the FDA?

NuFACE Mini Device received FDA 510(k) clearance on 2019-10-15, under approval number K191672.

What company makes NuFACE Mini Device?

NuFACE Mini Device is manufactured by Carol Cole Company Dba Nuface.

What is the FDA product code for NuFACE Mini Device?

The FDA product code for NuFACE Mini Device is NFO.

Other Devices by Carol Cole Company Dba Nuface

K171588NuBODY Skin Toning Device K182424NuFACE FIX Skin Toning Device K181008NuFACE Trinity K201906Trinity ELE Plus and Trinity ELE Plus Pro K201782NuFace Trinity Plus Device K212947Trinity Plus Wrinkle Reducer

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Related Devices (Code: NFO)

K152199RejuvatoneMDTrophy Skin, Inc. K150826Nutra Face Lift Model PE8050Nutra Luxe MD, LLC K163550Pobling MIITY 2Habalan Med & Beauty Co.,Ltd K162652Smart Photon Micro-current Device, Model: EP-300Li-Tek Electronic Technology Corporation K171647BeneLife Premium Facial Treatment Pack, Model: QZ0701AInfinitus (China) Company , Ltd. K171588NuBODY Skin Toning DeviceCarol Cole Company Dba Nuface

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.