CAO Group, Inc. - FDA 510(k) Cleared Devices
31
Total
31
Cleared
0
Denied
FDA 510(k) cleared devices by CAO Group, Inc. General & Plastic Surgery ✕
18 devices
Cleared
Mar 11, 2026
Picasso Pro Diode Laser (002-00460)
General & Plastic Surgery
78d
Cleared
Oct 28, 2020
Ultimate Contour, Ultimate Contour Mini
General & Plastic Surgery
147d
Cleared
Sep 10, 2019
Pioneer Elite Diode Laser
General & Plastic Surgery
448d
Cleared
Sep 10, 2019
Sterling Supreme Diode Laser
General & Plastic Surgery
448d
Cleared
Sep 09, 2019
Precise SHP Diode Laser
General & Plastic Surgery
447d
Cleared
Oct 20, 2017
Ultimate Contour, Ultimate Contour Mini
General & Plastic Surgery
193d
Cleared
Sep 22, 2017
Sterling Supreme Diode Laser
General & Plastic Surgery
81d
Cleared
Sep 21, 2016
Sterling 5W Diode Laser
General & Plastic Surgery
218d
Cleared
Sep 12, 2014
Pilot Pro Diode Laser
General & Plastic Surgery
30d
Cleared
Sep 12, 2014
Pilot Elite Diode Laser
General & Plastic Surgery
30d
Cleared
Sep 12, 2014
Pilot Ultra Diode Laser
General & Plastic Surgery
30d
Cleared
Sep 13, 2013
PIONEER ELITE DIODE LASER
General & Plastic Surgery
150d
Cleared
Aug 13, 2013
PRECISE SHP DIODE LASER
General & Plastic Surgery
278d
Cleared
Aug 30, 2012
PRECISE SHP DIODE LASER
General & Plastic Surgery
282d
Cleared
Aug 13, 2010
PILOT DIODE LASER, MODEL 002-00139
General & Plastic Surgery
206d
Cleared
Nov 14, 2006
DENLASER 800 PLUS
General & Plastic Surgery
70d
Cleared
Jul 10, 2006
DENLASER 800 PLUS
General & Plastic Surgery
55d
Cleared
Jan 25, 2001
DENLASER, MODEL 800
General & Plastic Surgery
70d