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Staple Driver

FDA product code HXJ · Class 1 · Orthopedic

27
Registered devices
1
Adverse events
2
Recalls
6
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2006-05-17Xiros PlcThe impactors are being recalled for modification so that they can be disassembled fully for cleaning and sterilization, on suspicion that the assembled items r
2006-05-17Xiros PlcThe impactors are being recalled for modification so that they can be disassembled fully for cleaning and sterilization, on suspicion that the assembled items r

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