Medical Device Manufacturer · US , Wayland , MA

Syneron Candela Corporation - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2016

Total

Cleared

Denied

Syneron Candela Corporation has 5 FDA 510(k) cleared medical devices. Based in Wayland, US.

Historical record: 5 cleared submissions from 2016 to 2017. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Syneron Candela Corporation Filter by specialty or product code using the sidebar.

Syneron Candela Corporation is one of 4717 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Syneron Candela Corporation

5 devices

1-5 of 5