Medical Device Manufacturer · US , Lake Forest , CA

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

6 submissions · 6 cleared · Since 1990

Total

Cleared

Denied

Sudormed, Inc. has 6 FDA 510(k) cleared medical devices. Based in Lake Forest, US.

Historical record: 6 cleared submissions from 1990 to 1996. Primary specialty: Toxicology.

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

Sudormed, 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 - Sudormed, Inc.

6 devices

1-6 of 6