NuFACE Trinity
K-Number: K181008 · 2018-10-11
ApplicantCarol Cole Company Dba Nuface
Decision Date2018-10-11
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
NuFACE Trinity is a medical device manufactured by Carol Cole Company Dba Nuface. It received FDA 510(k) clearance on 2018-10-11 under approval number K181008. 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?
NuFACE Trinity is a medical device that received FDA 510(k) clearance on 2018-10-11. It is manufactured by Carol Cole Company Dba Nuface. The 510(k) number is K181008.
When was NuFACE Trinity approved by the FDA?
NuFACE Trinity received FDA 510(k) clearance on 2018-10-11, under approval number K181008.
What company makes NuFACE Trinity?
NuFACE Trinity is manufactured by Carol Cole Company Dba Nuface.
What is the FDA product code for NuFACE Trinity?
The FDA product code for NuFACE Trinity is NFO.
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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.