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Forceps, Wire Holding

FDA product code HYA · Class 1 · General, Plastic Surgery

130
Registered devices
11
Adverse events
1
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2015-06-17Biomet, Inc.Medium Bone Plate Forceps was assembled with the incorrect grip arm tip. Potential that the surgeon will be unable to provisionally clamp the plate to the pati

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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.