Arthrex, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Arthrex Plates, Screws and Pins, and Washers, Arthrex FiberButton, Arthrex Beaming System
357
Total
353
Cleared
0
Denied
FDA 510(k) Regulatory Record - Arthrex, Inc. Orthopedic ✕
318 devices
Cleared
Oct 29, 2026
Arthrex Plates, Screws and Pins, and Washers
Orthopedic
29d
Cleared
Oct 27, 2026
Arthrex FiberButton
Orthopedic
28d
Cleared
Sep 25, 2026
Arthrex Beaming System
Orthopedic
30d
Cleared
Sep 24, 2026
Arthrex Spine Compression FT Screw
Orthopedic
58d
Cleared
Sep 01, 2026
Arthrex DynaNite Staples
Orthopedic
46d
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
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