Candela Corporation - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
FDA 510(k) cleared devices by Candela Corporation General & Plastic Surgery ✕
8 devices
Cleared
Jul 01, 2024
Profound Matrix
General & Plastic Surgery
174d
Cleared
Jun 01, 2023
Candela Vbeam Family of Pulsed Dye Lasers (Vbeam Prima, Vbeam Perfecta)
General & Plastic Surgery
56d
Cleared
Oct 13, 2022
PicoWay Laser System
General & Plastic Surgery
204d
Cleared
Dec 20, 2021
Frax 1940 for Nordlys and Frax Pro
General & Plastic Surgery
133d
Cleared
Dec 16, 2021
Profound Matrix
General & Plastic Surgery
237d
Cleared
May 26, 2020
GentleMax Pro Plus
General & Plastic Surgery
29d
Cleared
Sep 16, 2019
PicoWay Laser System
General & Plastic Surgery
84d
Cleared
Apr 16, 2015
PicoWay Laser System
General & Plastic Surgery
66d