Medical Device Manufacturer · US , Buffalo , NY

Leica, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1992

Total

Cleared

Denied

Leica, Inc. has 3 FDA 510(k) cleared medical devices. Based in Buffalo, US.

Historical record: 3 cleared submissions from 1992 to 1995. Primary specialty: Ophthalmic.

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

Leica, Inc. 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 - Leica, Inc.

3 devices

1-3 of 3