Arthrex, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Arthrex Bioabsorbable PushLock Suture Anchors, Arthrex Radial Head Replacement System, Arthrex FiberButton
352
Total
348
Cleared
0
Denied
FDA 510(k) Regulatory Record - Arthrex, Inc. Orthopedic ✕
313 devices
Cleared
Aug 07, 2026
Arthrex Bioabsorbable PushLock Suture Anchors
Orthopedic
28d
Cleared
Jul 30, 2026
Arthrex Radial Head Replacement System
Orthopedic
154d
Cleared
Jun 26, 2026
Arthrex FiberButton
Orthopedic
172d
Cleared
Jun 25, 2026
Arthrex Sterile VAL and VAL KreuLock™ Compression Screw System
Orthopedic
105d
Cleared
May 28, 2026
Arthrex Bioabsorbable PushLock Suture Anchors
Orthopedic
170d
Cleared
May 08, 2026
Arthrex Beaming System
Orthopedic
130d
Cleared
Mar 20, 2026
Arthrex Humeral Nails
Orthopedic
266d
Cleared
Mar 20, 2026
Arthrex FiberTak Suture Anchor
Orthopedic
29d
Cleared
Mar 09, 2026
FiberTape Button
Orthopedic
28d
Cleared
Mar 05, 2026
Arthrex FibuLock Nail System
Orthopedic
234d
Cleared
Mar 03, 2026
Arthrex Humeral Plating System (Anatomic Humeral Plate) and Cerclage Button
Orthopedic
28d
Cleared
Mar 02, 2026
Arthrex Nano FiberTak Suture Anchor
Orthopedic
63d
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