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Anmuth Medical International

Anmuth Medical International, LLC · Model 39-541-23TC · UDI-DI 08403207010100

HXZ
1
510(k) clearances
510
Adverse events
1
Recalls
246
Facilities

Description

Side Wire Cutter D/A 23cm/9"

Recalls

DateFirmReason
2020-11-20Zimmer Biomet, Inc.Device has the potential for fracture during use.

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Data 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.