Medical Device Manufacturer · US , Winter Park , FL

Dannik - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2019

Total

Cleared

Denied

Dannik has 5 FDA 510(k) cleared medical devices. Based in Winter Park, US.

Historical record: 5 cleared submissions from 2019 to 2020. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) cleared devices by Dannik

5 devices

1-5 of 5