Medical Device Manufacturer · US , The Woodlands , TX

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

3 submissions · 3 cleared · Since 1993

Total

Cleared

Denied

Diomedics, Inc. has 3 FDA 510(k) cleared medical devices. Based in The Woodlands, US.

Historical record: 3 cleared submissions from 1993 to 2008. Primary specialty: General & Plastic Surgery.

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

Diomedics, 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 - Diomedics, Inc.

3 devices

1-3 of 3