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Arthrex®
ARTHREX, INC. · Model AR-9339-18 · UDI-DI 00888867059979
QHQ
Prescription
1
510(k) clearances
149
Adverse events
1
Recalls
19
Facilities
Description
ARTHREX ECLIPSE HUMERAL HEAD, 39/18
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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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.