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Rexious
DIOMEDICAL CO.,LTD. · Model A · UDI-DI 08800113943544
OUR
Prescription
1
510(k) clearances
1,406
Adverse events (5 deaths)
1
Recalls
154
Facilities
Description
Poly-Axial Pedicle L Type (Double & Self Tapping) (L1)55x(L2)9.5x(A)16.4x(B)13.5mm-Ø6.0
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-11-03 | Orthofix U.S. LLC | Labeling contains claims that are not consistently present. |
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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.