Syneron Candela Corporation - FDA 510(k) Cleared Devices

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.

510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.