Trinity Plus Wrinkle Reducer
K-Number: K212947 · 2022-04-02
ApplicantCarol Cole Company Dba Nuface
Decision Date2022-04-02
Product CodeOHS
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Trinity Plus Wrinkle Reducer is a medical device manufactured by Carol Cole Company Dba Nuface. It received FDA 510(k) clearance on 2022-04-02 under approval number K212947. The device is classified under product code OHS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Trinity Plus Wrinkle Reducer?
Trinity Plus Wrinkle Reducer is a medical device that received FDA 510(k) clearance on 2022-04-02. It is manufactured by Carol Cole Company Dba Nuface. The 510(k) number is K212947.
When was Trinity Plus Wrinkle Reducer approved by the FDA?
Trinity Plus Wrinkle Reducer received FDA 510(k) clearance on 2022-04-02, under approval number K212947.
What company makes Trinity Plus Wrinkle Reducer?
Trinity Plus Wrinkle Reducer is manufactured by Carol Cole Company Dba Nuface.
What is the FDA product code for Trinity Plus Wrinkle Reducer?
The FDA product code for Trinity Plus Wrinkle Reducer is OHS.
Other Devices by Carol Cole Company Dba Nuface
Related Devices (Code: OHS)
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.