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AESCULAP
AESCULAP, INC. · Model MG029R · UDI-DI 04046964573941
HXZ
Prescription
1
510(k) clearances
510
Adverse events
1
Recalls
246
Facilities
Description
Wire Cutting Forceps, 7", (180 mm), front and lateral cutting, non-sterile, reusable
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2020-11-20 | Zimmer Biomet, Inc. | Device has the potential for fracture during use. |
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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.