FDA Device Intelligence
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Starter, Bone Screw

FDA product code HWD · Class 1 · Orthopedic

225
Registered devices
28
Adverse events
1
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2011-03-10Biomet, Inc.One lot of 30 mm screws was switched with one lot of 25 mm screws.

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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.