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Anmuth Medical International
Anmuth Medical International, LLC · Model 39-541-21TC · UDI-DI 08403207010094
1
510(k) clearances
510
Adverse events
1
Recalls
246
Facilities
Description
WIRE CUT-SIDE CUT, TC 2.5MM ANG 8 1/2",D/A
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.