Arthrex, Inc.
FDA 510(k) & PMA Approved Devices — 173 products
Total Devices173
Categories29
Latest FDA decision2026-08-07
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K262357 | Arthrex Bioabsorbable PushLock Suture Anchors | MAI | 2026-08-07 | View |
| 510(k) | K260624 | Arthrex Radial Head Replacement System | KWI | 2026-07-30 | View |
| 510(k) | K260018 | Arthrex FiberButton | MBI | 2026-06-26 | View |
| 510(k) | K260809 | Arthrex Sterile VAL and VAL KreuLock™ Compression Screw System | HWC | 2026-06-25 | View |
| 510(k) | K253931 | Arthrex Bioabsorbable PushLock Suture Anchors | MAI | 2026-05-28 | View |
| 510(k) | K254215 | Arthrex Beaming System | HWC | 2026-05-08 | View |
| 510(k) | K252016 | Arthrex Humeral Nails | HSB | 2026-03-20 | View |
| 510(k) | K260561 | Arthrex FiberTak Suture Anchor | MBI | 2026-03-20 | View |
| 510(k) | K260405 | FiberTape Button | MBI | 2026-03-09 | View |
| 510(k) | K252196 | Arthrex FibuLock Nail System | HSB | 2026-03-05 | View |
| 510(k) | K260353 | Arthrex Humeral Plating System (Anatomic Humeral Plate) and Cerclage Button | HRS | 2026-03-03 | View |
| 510(k) | K254229 | Arthrex Nano FiberTak Suture Anchor | MBI | 2026-03-02 | View |
| 510(k) | K253713 | Arthrex Variable Angle (VA) Proximal Tibia Plating System | HRS | 2026-01-21 | View |
| 510(k) | K252807 | Arthrex Anatomic Lapidus Plates and I-Beam Lapidus Plates | HRS | 2026-01-12 | View |
| 510(k) | K253895 | Arthrex SwiveLock Suture Anchor, 3.5 x 10 mm | MBI | 2025-12-30 | View |
| 510(k) | K253727 | Syndesmosis TightRope PRO | HTN | 2025-12-22 | View |
| 510(k) | K252314 | Arthrex SutureTak Suture Anchor | MBI | 2025-10-29 | View |
| 510(k) | K251994 | Arthrex Synergy Vision Imaging System | GCJ | 2025-10-16 | View |
| 510(k) | K251690 | Arthrex SpeedFLEX™ Implant | OWY | 2025-09-30 | View |
| 510(k) | K251809 | Arthrex FiberTak Suture Anchor | MBI | 2025-07-18 | View |
No matching devices.
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Related Clinical Trials
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