Carol Cole Company is one of 4737 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Carol Cole Company - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Carol Cole Company has 6 FDA 510(k) cleared medical devices. Based in La Jolla, US.
Historical record: 6 cleared submissions from 2007 to 2016. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Carol Cole Company Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Carol Cole Company
6 devices
Cleared
Dec 30, 2016
NuFACE Gel Primer
Neurology
198d
Cleared
Apr 17, 2014
NUFACE MINI DEVICE
Neurology
121d
Cleared
Oct 01, 2013
TRINITY ELE
Neurology
153d
Cleared
Nov 06, 2012
TRINITY WRINKLE REMOVER
General & Plastic Surgery
256d
Cleared
Nov 07, 2011
NUFACE PLUS
Neurology
348d
Cleared
Nov 27, 2007
NUFACE, MODEL NU-4003
Neurology
105d