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Bone Mill

FDA product code LYS · Class 1 · Orthopedic

266
Registered devices
1,273
Adverse events
1
Recalls
4
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2006-10-20Medtronic Sofamor Danek USA IncMetal bone fragmentor was causing metal shavings to be released into the resultant fragmented tissue 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.