Medical Device Manufacturer · US , Washington , DC

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

1 submissions · 1 cleared · Since 2003

Total

Cleared

Denied

Genosis, Inc. has 1 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: Chemistry.

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

Genosis, 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 - Genosis, Inc.

1 devices

1-1 of 1