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Cutter, Wire

FDA product code HXZ · Class 1 · Orthopedic

986
Registered devices
510
Adverse events
1
Recalls
1
510(k) clearances

Devices with this code

Recent recalls

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

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.