ClearanceBrief
Company · US

Carol Cole Company Dba Nuface

FDA 510(k) clearances and medical device recalls filed under this name, 2017 to 2024. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
NFOStimulator, Transcutaneous Electrical, Aesthetic Purposes7
OHSLight Based Over The Counter Wrinkle Reduction1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 27, 2024K240564NuFACE® FIX+
Carol Cole Company Dba Nuface®
NFO
Apr 2, 2022K212947Trinity Plus Wrinkle Reducer
Carol Cole Company Dba Nuface
OHS
Feb 24, 2021K201906Trinity ELE Plus and Trinity ELE Plus Pro
Carol Cole Company Dba Nuface
NFO
Jan 22, 2021K201782NuFace Trinity Plus Device
Carol Cole Company Dba Nuface
NFO
Oct 15, 2019K191672NuFACE Mini Device
Carol Cole Company Dba Nuface
NFO
Dec 18, 2018K182424NuFACE FIX Skin Toning Device
Carol Cole Company Dba Nuface
NFO
Oct 11, 2018K181008NuFACE Trinity
Carol Cole Company Dba Nuface
NFO
Jul 31, 2017K171588NuBODY Skin Toning Device
Carol Cole Company Dba Nuface
NFO

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
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