Orison Corporation is one of 22849 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Orison Corporation - FDA 510(k) Cleared Devices
Recent clearances: EMBRACE GEL, ORISON EMBRACE SYSTEM
2
Total
2
Cleared
0
Denied
Orison Corporation has 2 FDA 510(k) cleared medical devices. Based in Johnson City, US.
Historical record: 2 cleared submissions from 2007 to 2007. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Orison Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Orison Corporation
2 devices