Medical Device Manufacturer · US , Irvine , CA

Biovision AG - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2002

Total

Cleared

Denied

Biovision AG has 2 FDA 510(k) cleared medical devices. Based in Irvine, US.

Historical record: 2 cleared submissions from 2002 to 2004. Primary specialty: Ophthalmic.

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

Biovision AG is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Biovision AG

2 devices

1-2 of 2