Medical Device Manufacturer · US , Washington , DC

Sargon Ent., Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1994

Total

Cleared

Denied

Sargon Ent., Inc. has 3 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 3 cleared submissions from 1994 to 2010. Primary specialty: Dental.

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

Sargon Ent., 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 - Sargon Ent., Inc.

3 devices

1-3 of 3