Medical Device Manufacturer · US , Bay Shore , NY

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

8 submissions · 8 cleared · Since 1990

Total

Cleared

Denied

Lumex, Inc. has 8 FDA 510(k) cleared medical devices. Based in Bay Shore, US.

Historical record: 8 cleared submissions from 1990 to 1997. Primary specialty: General Hospital.

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

Lumex, 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 - Lumex, Inc.

8 devices

1-8 of 8