Medical Device Manufacturer · IT , Dueville (Vi)

Biotec Italia, Srl - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2022

Total

Cleared

Denied

Biotec Italia, Srl has 1 FDA 510(k) cleared medical devices. Based in Dueville (Vi), IT.

Last cleared in 2022. Active since 2022. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Biotec Italia, Srl Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Biotec Italia, Srl

1 devices

1-1 of 1