BEUDAMED
    3 results · 14ms · 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 Status: Malfunction ×

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·March 2, 2023

    INCLUSIVE TAPERED IMPLANT 5.2 X 13MM

    FDA Adverse Event
    Malfunction ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·May 20, 2014

    ZERO TIP STONE RETRIEVAL BASKET

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code FFL·August 12, 2010