BEUDAMED
    FDA Adverse Event Injury Summary report: N

    C1-11330

    MDR report key: 23468063 · Received November 4, 2025

    Report

    Report Number
    3004203816-2025-41729
    Event Type
    Injury
    Date Received
    November 4, 2025
    Report Date
    November 4, 2025
    Manufacturer
    MIS IMPLANTS TECHNOLOGIES LTD.
    Product Code
    DZE
    UDI-DI
    07290108992137
    PMA / PMN Number
    K172505
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    RS
    Reporter Occupation
    003

    Narratives

    Additional Manufacturer Narrative · 0

    SINCE THIS EVENT RESULTED IN A SERIOUS INJURY, IT IS REPORTABLE PER 21 CFR PART 803. THE DEVICE WAS NOT EVALUATED BECAUSE THE ISSUE IS A KNOWN INHERENT RISK OF THE DEVICE. WE WILL CONTINUE TO TRACK AND MONITOR THE TREND.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1841138 C1-11330 IMPLANT, ENDOSSEOUS, ROOT-FORM DZE MIS IMPLANTS TECHNOLOGIES LTD. W24011883 07290108992137

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Female Required Intervention