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Brace, Drill

FDA product code HXY · Class 1 · Orthopedic

159
Registered devices
44
Adverse events
1
Recalls
7
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2015-05-27Musculoskeletal Transplant Foundation, Inc.Musculoskeletal Transplant Foundation is recalling a certain lot of Allofix Insertion Kits because they are labeled as having a 2.0mm diameter drill however it

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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.