NuFace Trinity Plus Device
K-Number: K201782 · 2021-01-22
Device Summary
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. The listed applicant is Carol Cole Company Dba Nuface. The 510(k) number is K201782.
When did NuFace Trinity Plus Device receive FDA 510(k) clearance?
NuFace Trinity Plus Device received FDA 510(k) clearance on 2021-01-22, under 510(k) number K201782.
Who is the listed applicant for NuFace Trinity Plus Device?
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 NuFace Trinity Plus Device?
The FDA product code for NuFace Trinity Plus Device is NFO.
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: NFO)
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.