Trinity Plus Wrinkle Reducer
K-Number: K212947 · 2022-04-02
Device Summary
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. The listed applicant is Carol Cole Company Dba Nuface. The 510(k) number is K212947.
When did Trinity Plus Wrinkle Reducer receive FDA 510(k) clearance?
Trinity Plus Wrinkle Reducer received FDA 510(k) clearance on 2022-04-02, under 510(k) number K212947.
Who is the listed applicant for Trinity Plus Wrinkle Reducer?
The FDA 510(k) record lists Carol Cole Company Dba Nuface as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Trinity Plus Wrinkle Reducer?
The FDA product code for Trinity Plus Wrinkle Reducer is OHS.
Other records listing Carol Cole Company Dba Nuface as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: OHS)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.