Arex USA is one of 20554 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Arex USA - FDA 510(k) Cleared Devices
Recent clearances: LIGAMENTOTAXOR, AREX SCRU 2 HEADLESS COMPRESSION SCREWS, MODELS: P2P10, P2P15, P2P20, P2P25, P2P30, P2P35, P2P40, P2P45
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.
FDA 510(k) Regulatory Record - Arex USA
2 devices