Home › Biomet Orthopedics, LLC › ULTRA-DRIVE TOOL
ULTRA-DRIVE TOOL
Biomet Orthopedics, LLC · Model 423856 · UDI-DI 00880304000698
JXE
Prescription
1
510(k) clearances
93
Adverse events
1
Recalls
28
Facilities
Description
56 MM X 85 DEGREE ACETABULAR GOUGE
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2012-04-18 | Biomet, Inc. | Incorrect product picture label was on the product box. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData 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.