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ULTRA DRIVE III CONSOLE

Biomet Orthopedics, LLC · Model 423935 · UDI-DI 00880304467293

JXEJDX Prescription
1
510(k) clearances
93
Adverse events
1
Recalls
28
Facilities

Recalls

DateFirmReason
2012-04-18Biomet, Inc.Incorrect product picture label was on the product box.

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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.