Medical Device Manufacturer · IT , Via Belvedere, 18

Polinelli - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1987

Total

Cleared

Denied

Polinelli has 2 FDA 510(k) cleared medical devices. Based in Via Belvedere, 18, IT.

Historical record: 2 cleared submissions from 1987 to 1987. Primary specialty: Ophthalmic.

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

Polinelli 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 - Polinelli

2 devices

1-2 of 2