Medical Device Manufacturer · US , Lansing , MI

Surgi-Med, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1987

Total

Cleared

Denied

Surgi-Med, Inc. has 5 FDA 510(k) cleared medical devices. Based in Lansing, US.

Historical record: 5 cleared submissions from 1987 to 1988. Primary specialty: General Hospital.

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

Surgi-Med, 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 - Surgi-Med, Inc.

5 devices

1-5 of 5