BEUDAMED
    FDA Adverse Event Injury Summary report: N

    INTERPORE IMZ IMPLANT

    MDR report key: 42384 · Received October 10, 1996

    Report

    Report Number
    2029012-1996-00011
    Event Type
    Injury
    Date Received
    October 10, 1996
    Date of Event
    September 9, 1996
    Report Date
    October 9, 1996
    Manufacturer
    INTERPORE INTL
    Product Code
    DZE
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IN, US
    Reporter Occupation
    DENTIST

    Narratives

    Description of Event or Problem · 1

    IMPLANT WAS EXPLANED DUE TO INADEQUATE OSTEOINTEGRATION. BONE LOSS WAS NOTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 INTERPORE IMZ IMPLANT Implant ENDOSSEOUS DENTAL IMPLANT DZE INTERPORE INTL NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Required Intervention