Medical Device Manufacturer · US , Wayland , MA

Candela Laser Corp. - FDA 510(k) Cleared Devices

43 submissions · 43 cleared · Since 1988
43
Total
43
Cleared
0
Denied

Candela Laser Corp. has 43 FDA 510(k) cleared medical devices. Based in Wayland, US.

Historical record: 43 cleared submissions from 1988 to 1996. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) cleared devices by Candela Laser Corp.

43 devices
1-12 of 43

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