Medical Device Manufacturer · FI , Helsinki

Orion Corporation Soredex - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1988

Total

Cleared

Denied

Orion Corporation Soredex has 4 FDA 510(k) cleared medical devices. Based in Helsinki, FI.

Historical record: 4 cleared submissions from 1988 to 1998. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Orion Corporation Soredex Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Orion Corporation Soredex

4 devices

1-4 of 4