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AESCULAP
AESCULAP, INC. · Model MB410R · UDI-DI 04046964567278
EMM
Prescription
4
510(k) clearances
2
Adverse events
1
Recalls
132
Facilities
Description
OSTEOTOME HEX HDL BLADE 8MM 160MM
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2008-04-16 | Biomet Microfixation, Inc. | The working tips of the Stella Osteotomes are thicker than specification. |
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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.
