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Bilateral BMA Kit

Biomet Biologics, LLC · Model 800-0710 · UDI-DI 00880304640962

LWE Prescription
3
510(k) clearances
46
Adverse events
1
Recalls
21
Facilities

Recalls

DateFirmReason
2010-10-18Orthofix IncOuter cartons for the product may be labeled with incorrect needle gauge.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data 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.