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Vernier

UNITED ORTHOPEDIC CORP. · Model 9401-7011 · UDI-DI 04711605582599

KTZ Prescription
7
510(k) clearances
14
Adverse events
0
Recalls
194
Facilities

Description

U2 Total Knee System

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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.