Home › Biomet Orthopedics, LLC › IM INTERNAL CHISEL
IM INTERNAL CHISEL
Biomet Orthopedics, LLC · Model 475730 · UDI-DI 00880304386631
FZO
Prescription
2
510(k) clearances
315
Adverse events
1
Recalls
244
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2015-06-24 | Synthes (USA) Products LLC | It was discovered that a 10mm Chisel Blade was etched as a 16mm Chisel Blade. |
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.