Arthrex, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Arthrex Bioabsorbable PushLock Suture Anchors, Arthrex Beaming System, Arthrex Humeral Nails
348
Total
344
Cleared
0
Denied
FDA 510(k) Regulatory Record - Arthrex, Inc. Orthopedic ✕
309 devices
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
Cleared
Jan 21, 2026
Arthrex Variable Angle (VA) Proximal Tibia Plating System
Orthopedic
58d
Cleared
Jan 12, 2026
Arthrex Anatomic Lapidus Plates and I-Beam Lapidus Plates
Orthopedic
131d
Cleared
Dec 30, 2025
Arthrex SwiveLock Suture Anchor, 3.5 x 10 mm
Orthopedic
26d
Cleared
Dec 22, 2025
Syndesmosis TightRope PRO
Orthopedic
28d
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