Medical Device Manufacturer · US , North Attleboro , MA

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

4 submissions · 4 cleared · Since 1998

Total

Cleared

Denied

Euromed, Inc. has 4 FDA 510(k) cleared medical devices. Based in North Attleboro, US.

Historical record: 4 cleared submissions from 1998 to 2008. Primary specialty: General & Plastic Surgery.

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

Euromed, 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 - Euromed, Inc.

4 devices

1-4 of 4