Medical Device Manufacturer · US , Wayland , MA

Syneron Candela Corporation - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2016

Recent clearances: PicoWay Laser System, PicoWay Laser System, Profound System

View 5 510(k) Devices ↓
5
Total
5
Cleared
0
Denied

FDA 510(k) Regulatory Record - Syneron Candela Corporation General & Plastic Surgery ✕

5 devices
1-5 of 5
Cleared May 25, 2017
PicoWay Laser System
K170597 · GEX
General & Plastic Surgery · 86d
Cleared Feb 01, 2017
PicoWay Laser System
K162454 · GEX
General & Plastic Surgery · 153d
Cleared CT Sep 12, 2016
Profound System
K161043 · PBX
General & Plastic Surgery · 152d
Cleared Jul 05, 2016
PicoWay Laser System
K160607 · GEX
General & Plastic Surgery · 125d
Cleared Mar 02, 2016
PicoWay Laser System
K153527 · GEX
General & Plastic Surgery · 84d
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