Arex USA - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Arex USA has 2 FDA 510(k) cleared medical devices. Based in Collegeville, US.
Historical record: 2 cleared submissions from 2008 to 2010. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Arex USA Filter by specialty or product code using the sidebar.
2 devices