CAO Group, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
CAO Group, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Picasso Pro Diode Laser (002-00460), Monet Curing Laser, Ultimate Contour, Ultimate Contour Mini
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.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - 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
CT
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