Cynosure, LLC - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Cynosure, LLC has 7 FDA 510(k) cleared medical devices. Based in Wesford, US.
Latest FDA clearance: Mar 2024. Active since 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Cynosure, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Cynosure, LLC
7 devices
Cleared
Mar 08, 2024
Elite iQ PRO (M122K1)
General & Plastic Surgery
29d
Cleared
Jul 06, 2023
MyEllevate
General & Plastic Surgery
132d
Cleared
Nov 23, 2022
TempSure System
General & Plastic Surgery
28d
Cleared
Mar 18, 2022
TempSure System
General & Plastic Surgery
189d
Cleared
Mar 30, 2021
PicoSure Workstation
General & Plastic Surgery
61d
Cleared
Mar 25, 2020
TempSure System
General & Plastic Surgery
54d
Cleared
Mar 09, 2020
Elite iQ
General & Plastic Surgery
90d