ClearanceBrief
Company ยท US

Carol Cole Company

FDA 510(k) clearances and medical device recalls filed under this name, 2007 to 2016. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
NFOStimulator, Transcutaneous Electrical, Aesthetic Purposes4
GYBMedia, Electroconductive1
OHSLight Based Over The Counter Wrinkle Reduction1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Dec 30, 2016K161654NuFACE Gel Primer
Carol Cole Company
GYB
Apr 17, 2014K133823NUFACE MINI DEVICE
Carol Cole Company
NFO
Oct 1, 2013K131251TRINITY ELE
Carol Cole Company
NFO
Nov 6, 2012K120560TRINITY WRINKLE REMOVER
Carol Cole Company
OHS
Nov 7, 2011K103472NUFACE PLUS
Carol Cole Company
NFO
Nov 27, 2007K072260NUFACE, MODEL NU-4003
Carol Cole Company
NFO

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes