Candela Corpation is one of 19064 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Candela Corpation - FDA 510(k) Cleared Devices
Recent clearances: Pico Way Laser System
1
Total
1
Cleared
0
Denied
Candela Corpation has 1 FDA 510(k) cleared medical devices. Based in Wayland, US.
Historical record: 1 cleared submissions from 2014 to 2014. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Candela Corpation 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.
FDA 510(k) Regulatory Record - Candela Corpation
1 devices