CAO Group, Inc. - FDA 510(k) Cleared Devices
31
Total
31
Cleared
0
Denied
CAO Group, Inc. has 31 FDA 510(k) cleared medical devices. Based in West Jordan, US.
Latest FDA clearance: Mar 2026. Active since 2001. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by CAO Group, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by CAO Group, Inc.
31 devices
Cleared
Mar 11, 2026
Picasso Pro Diode Laser (002-00460)
General & Plastic Surgery
78d
Cleared
Nov 24, 2020
Monet Curing Laser
Dental
138d
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
Dec 31, 2015
Ascent 3D
Dental
297d
Cleared
Sep 12, 2014
Pilot Pro Diode Laser
General & Plastic Surgery
30d
Cleared
Sep 12, 2014
Pilot Elite Diode Laser
General & Plastic Surgery
30d