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Crimper, Pin

FDA product code HXQ · Class 1 · Orthopedic

49
Registered devices
13
Adverse events
1
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2014-09-26Biomet, Inc.An investigation identified that high level friction may exist between the needle and Mamba suture passer instrument, causing the needle to break 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.