BEUDAMED
    FDA Adverse Event Injury Summary report: N

    Z-LOOK3

    MDR report key: 3171396 · Received June 15, 2013

    Report

    Report Number
    3006948427-2013-00506
    Event Type
    Injury
    Date Received
    June 15, 2013
    Date of Event
    May 16, 2011
    Report Date
    May 21, 2013
    Manufacturer
    Z-SYSTEMS AG
    Product Code
    DZE
    PMA / PMN Number
    K062542
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OK, US
    Reporter Occupation
    DENTIST

    Narratives

    Description of Event or Problem · 1

    DENTAL IMPLANT DID NOT OSSEOINTEGRATE AND HAD TO BE REMOVED AFTER PROSTHETIC TREATMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    272683 Z-LOOK3 ENDOSSEOUS DENTAL IMPLANT ROOT FORM DZE Z-SYSTEMS AG Z3-36-11 10429

    Patients

    Seq Age Sex Outcome Treatment
    1 27 YR Other