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N/A
BIOMET MICROFIXATION, INC · Model 01-8264 · UDI-DI 00841036016296
KAD
Prescription
5
510(k) clearances
21
Adverse events
1
Recalls
120
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-12-03 | Sklar Instruments | Reports of various packaging issues that may result in a breach of the sterile barrier. |
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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.