Medical Device Manufacturer · IT , Treviso, Italy

Venis DI A. Vendrame - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1993

Total

Cleared

Denied

Venis DI A. Vendrame has 1 FDA 510(k) cleared medical devices. Based in Treviso, Italy, IT.

Historical record: 1 cleared submissions from 1993 to 1993. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Venis DI A. Vendrame Filter by specialty or product code using the sidebar.

Venis DI A. Vendrame is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Venis DI A. Vendrame

1 devices

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