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Bone Sonometer

FDA product code MUA · Class 2 · Radiology

18
Registered devices
1
Adverse events
2
Recalls
9
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2019-09-03GE Healthcare, LLCCertain Achilles Express and Achilles Insight systems were shipped with European CEE-7/7 Type Power Cords to countries where three protruding pin plugs are requ
2019-09-03GE Healthcare, LLCCertain Achilles Express and Achilles Insight systems were shipped with European CEE-7/7 Type Power Cords to countries where three protruding pin plugs are requ

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