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AESCULAP
AESCULAP, INC. · Model MB892R · UDI-DI 04046964582776
EXX
Prescription
0
510(k) clearances
10
Adverse events
1
Recalls
41
Facilities
Description
STEWART Crypt Hook, 9", (230 mm), (29 mm)
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2009-04-09 | Marina Medical Instruments Inc. | Marina Medical, Sunrise, FL initiated recall of 46 different 350 series devices and 47 different 270 series products because the material used to manufacture the products was not p |
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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.
