Cutera, Inc. - FDA 510(k) Cleared Devices
31
Total
31
Cleared
0
Denied
Cutera, Inc. has 31 FDA 510(k) cleared medical devices. Based in Brisbane, US.
Latest FDA clearance: Jul 2025. Active since 2004.
Browse the FDA 510(k) cleared devices submitted by Cutera, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Cutera, Inc.
6 devices
Cleared
Jul 11, 2025
AviClear Laser System
General & Plastic Surgery
88d
Cleared
Dec 15, 2023
xeo+ Family
General & Plastic Surgery
78d
Cleared
Jun 06, 2023
AviClear Laser System
General & Plastic Surgery
88d
Cleared
Nov 03, 2022
truSculpt iD
General & Plastic Surgery
31d
Cleared
Jul 13, 2022
truSculpt iD
General & Plastic Surgery
58d
Cleared
Mar 24, 2022
AviClear Laser System
General & Plastic Surgery
148d