Medical Device Manufacturer · US , Meridian , TX

Scion International, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1996

Total

Cleared

Denied

Scion International, Inc. has 4 FDA 510(k) cleared medical devices. Based in Meridian, US.

Historical record: 4 cleared submissions from 1996 to 2004. Primary specialty: General & Plastic Surgery.

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

Scion International, 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 - Scion International, Inc.

4 devices

1-4 of 4