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GPS® III

Biomet Biologics, LLC · Model 800-0745 · UDI-DI 00880304460652

KSS Prescription
6
510(k) clearances
72
Adverse events
0
Recalls
39
Facilities

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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.