BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    KETAC-BOND APLICAP

    FDA 510(k)
    FDA Class 2 ·Dental

    SOLEO SUNBED

    FDA 510(k)

    ACUSON AL538 TRANSDUCER

    FDA 510(k)
    FDA Class 2 ·Radiology

    CS100

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP·Product code DSP·April 25, 2014

    CONSULTA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code NIK·October 19, 2010

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·December 16, 2012

    UNKNOWN GEL IMPLANTS

    FDA Adverse Event
    Injury ·MENTOR MEDICAL SYSTEM B.V.·Product code FTR·February 20, 2025

    UNKNOWN GEL IMPLANTS

    FDA Adverse Event
    Injury ·MENTOR MEDICAL SYSTEM B.V.·Product code FTR·February 20, 2025