BEUDAMED
    FDA Adverse Event Injury Summary report: N

    C1-13330

    MDR report key: 24465614 · Received February 26, 2026

    Report

    Report Number
    3004203816-2026-06191
    Event Type
    Injury
    Date Received
    February 26, 2026
    Report Date
    February 26, 2026
    Manufacturer
    MIS IMPLANTS TECHNOLOGIES LTD.
    Product Code
    DZE
    UDI-DI
    07290108992120
    PMA / PMN Number
    K172505
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SP
    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
    512191 C1-13330 IMPLANT, ENDOSSEOUS, ROOT-FORM DZE MIS IMPLANTS TECHNOLOGIES LTD. W23003354 07290108992120

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Male Required Intervention NOT PROVIDED