Home › Device types › QHQ
Total Shoulder Arthroplasty System
FDA product code QHQ · Class 2 · Orthopedic
78
Registered devices
148
Adverse events
1
Recalls
1
510(k) clearances
Devices with this code
Arthrex® — ARTHREX, INC.Arthrex® — ARTHREX, INC.Arthrex® — ARTHREX, INC.Arthrex® — ARTHREX, INC.Arthrex® — ARTHREX, INC.Arthrex® — ARTHREX, INC.Arthrex® — ARTHREX, INC.Arthrex® — ARTHREX, INC.Arthrex® — ARTHREX, INC.Arthrex® — ARTHREX, INC.Arthrex® — ARTHREX, INC.Arthrex® — ARTHREX, INC.Arthrex® — ARTHREX, INC.Arthrex® — ARTHREX, INC.Arthrex® — ARTHREX, INC.Arthrex® — ARTHREX, INC.Arthrex® — ARTHREX, INC.Arthrex® — ARTHREX, INC.Arthrex® — ARTHREX, INC.Arthrex® — ARTHREX, INC.Arthrex® — ARTHREX, INC.Arthrex® — ARTHREX, INC.Arthrex® — ARTHREX, INC.Arthrex® — ARTHREX, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-05-20 | Onkos Surgical, Inc. | Required inspections were not performed on finished product prior to release and distribution. |
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