NuBODY Skin Toning Device
K-Number: K171588 · 2017-07-31
Device Summary
Frequently Asked Questions
What is the NuBODY Skin Toning Device?
NuBODY Skin Toning Device is a medical device that received FDA 510(k) clearance on 2017-07-31. The listed applicant is Carol Cole Company Dba Nuface. The 510(k) number is K171588.
When did NuBODY Skin Toning Device receive FDA 510(k) clearance?
NuBODY Skin Toning Device received FDA 510(k) clearance on 2017-07-31, under 510(k) number K171588.
Who is the listed applicant for NuBODY Skin Toning 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 NuBODY Skin Toning Device?
The FDA product code for NuBODY Skin Toning 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.