FDA Device Intelligence
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Headrest, Neurosurgical

FDA product code HBM · Class 1 · Neurology

143
Registered devices
94
Adverse events
2
Recalls
3
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2023-12-12Steris CorporationDual-articulating head rest may not stay in place or may fail to lock into position during a patient procedure which could result in an injury to the patient or
2023-12-12Steris CorporationDual-articulating head rest may not stay in place or may fail to lock into position during a patient procedure which could result in an injury to the patient or

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