NuFACE Mini Device
K-Number: K191672 · 2019-10-15
Device Summary
Frequently Asked Questions
What is the NuFACE Mini Device?
NuFACE Mini Device is a medical device that received FDA 510(k) clearance on 2019-10-15. The listed applicant is Carol Cole Company Dba Nuface. The 510(k) number is K191672.
When did NuFACE Mini Device receive FDA 510(k) clearance?
NuFACE Mini Device received FDA 510(k) clearance on 2019-10-15, under 510(k) number K191672.
Who is the listed applicant for NuFACE Mini 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 Mini Device?
The FDA product code for NuFACE Mini 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.