Medical Device Manufacturer · IT , Italy

Lem Srl. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1987

Total

Cleared

Denied

Lem Srl. has 2 FDA 510(k) cleared medical devices. Based in Italy, IT.

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

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

Lem Srl. 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 - Lem Srl.

2 devices

1-2 of 2