Medical Device Manufacturer · IT , Italy

Castellini S.P.A. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1994

Total

Cleared

Denied

Castellini S.P.A. has 4 FDA 510(k) cleared medical devices. Based in Italy, IT.

Historical record: 4 cleared submissions from 1994 to 2003. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Castellini S.P.A. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Castellini S.P.A.

4 devices

1-4 of 4