NuFace Trinity Plus Device
K-Number: K201782 · 2021-01-22
ApplicantCarol Cole Company Dba Nuface
Decision Date2021-01-22
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
NuFace Trinity Plus Device is a medical device manufactured by Carol Cole Company Dba Nuface. It received FDA 510(k) clearance on 2021-01-22 under approval number K201782. 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 Trinity Plus Device?
NuFace Trinity Plus Device is a medical device that received FDA 510(k) clearance on 2021-01-22. It is manufactured by Carol Cole Company Dba Nuface. The 510(k) number is K201782.
When was NuFace Trinity Plus Device approved by the FDA?
NuFace Trinity Plus Device received FDA 510(k) clearance on 2021-01-22, under approval number K201782.
What company makes NuFace Trinity Plus Device?
NuFace Trinity Plus Device is manufactured by Carol Cole Company Dba Nuface.
What is the FDA product code for NuFace Trinity Plus Device?
The FDA product code for NuFace Trinity Plus Device is NFO.
Other Devices by Carol Cole Company Dba Nuface
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.