Medical Device Manufacturer · US , Hicksville , NY

Genadyne Biotechnologies - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2019

Total

Cleared

Denied

Genadyne Biotechnologies has 2 FDA 510(k) cleared medical devices. Based in Hicksville, US.

Historical record: 2 cleared submissions from 2019 to 2020. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) cleared devices by Genadyne Biotechnologies

2 devices

1-2 of 2