Medical Device Manufacturer · US , Brisbane , CA

Cutera, Inc. - FDA 510(k) Cleared Devices

31 submissions · 31 cleared · Since 2004
31
Total
31
Cleared
0
Denied

FDA 510(k) cleared devices by Cutera, Inc. General & Plastic Surgery ✕

30 devices
1-12 of 30
Cleared Jul 11, 2025
AviClear Laser System
K251149 · GEX
General & Plastic Surgery · 88d
Cleared Dec 15, 2023
xeo+ Family
K233237 · GEX
General & Plastic Surgery · 78d
Cleared Jun 06, 2023
AviClear Laser System
K230660 · GEX
General & Plastic Surgery · 88d
Cleared Nov 03, 2022
truSculpt iD
K223110 · GEI
General & Plastic Surgery · 31d
Cleared Jul 13, 2022
truSculpt iD
K221407 · GEI
General & Plastic Surgery · 58d
Cleared Mar 24, 2022
AviClear Laser System
K213461 · GEX
General & Plastic Surgery · 148d
Cleared Dec 12, 2018
enlighten III Laser System
K182997 · GEX
General & Plastic Surgery · 43d
Cleared Jun 06, 2018
truSculpt RF Device
K180709 · PBX
General & Plastic Surgery · 79d
Cleared Oct 27, 2017
Cutera enlighten III Laser System
K172077 · GEX
General & Plastic Surgery · 109d
Cleared Aug 02, 2017
truSculpt
K172004 · PBX
General & Plastic Surgery · 30d
Cleared Apr 25, 2017
Cutera enlighten III Laser System
K170936 · GEX
General & Plastic Surgery · 26d
Cleared Dec 09, 2016
truSculpt
K162512 · PBX
General & Plastic Surgery · 92d
Filters
Filter by Specialty
All31 General & Plastic Surgery 30 Physical Medicine 1