Medical Device Manufacturer · US , Medway , MA

Device Labs, Inc. - FDA 510(k) Cleared Devices

6 submissions · 5 cleared · Since 1988

Total

Cleared

Denied

Device Labs, Inc. has 5 FDA 510(k) cleared medical devices. Based in Medway, US.

Historical record: 5 cleared submissions from 1988 to 1993. Primary specialty: General Hospital.

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

Device Labs, 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 - Device Labs, Inc.

6 devices

1-6 of 6