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Ultra-Drive® Tool

Biomet Orthopedics, LLC · Model 423826 · UDI-DI 00887868560880

JDXJXE Prescription
1
510(k) clearances
175
Adverse events
2
Recalls
36
Facilities

Recalls

DateFirmReason
2019-06-04Zimmer Biomet, Inc.The products do not have sufficient data to support the labeled shelf life of 10 years.
2019-06-04Zimmer Biomet, Inc.The products do not have sufficient data to support the labeled shelf life of 10 years.

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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.