Arthex, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Arthex, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Arthrex SynergyID Endoscopic Imaging System
3
Total
3
Cleared
0
Denied
Arthex, Inc. has 3 FDA 510(k) cleared medical devices. Based in Naples, US.
Last cleared in 2023. Active since 2015. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Arthex, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Arthex, Inc.
3 devices