Aribex, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Aribex, Inc. has 3 FDA 510(k) cleared medical devices. Based in Orem, US.
Historical record: 3 cleared submissions from 2005 to 2014. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Aribex, Inc. Filter by specialty or product code using the sidebar.
3 devices