Medical Device Manufacturer · US , Plymouth , MN

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

2 submissions · 2 cleared · Since 2011

Total

Cleared

Denied

Superdimension, Inc. has 2 FDA 510(k) cleared medical devices. Based in Plymouth, US.

Historical record: 2 cleared submissions from 2011 to 2012. Primary specialty: Radiology.

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

FDA 510(k) Regulatory Record - Superdimension, Inc.

2 devices

1-2 of 2