BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ONYX IMPLANT

    MDR report key: 21410026 · Received February 19, 2025

    Report

    Report Number
    3012141159-2025-00023
    Event Type
    Injury
    Date Received
    February 19, 2025
    Date of Event
    October 10, 2024
    Report Date
    February 19, 2025
    Manufacturer
    NORIS MEDICAL LTD
    Product Code
    DZE
    UDI-DI
    07290108813104
    Adverse Event
    Yes
    Report Source
    Distributor report
    Reporter Location
    US
    Reporter Occupation
    DENTIST
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    A HEALTHCARE PROFESSIONAL REPORTED THAT NM-G3713 LOT#9000271 IMPLANT LACKED PRIMARY STABILITY DUE TO BONE TOO SOFT. THE IMPLANT WAS REMOVED DURING IMPLANT PLACEMENT WITH NO REPORT OF OBSERVABLE CLINICAL SYMPTOMS. ACCORDING TO THE INFORMATION, THE PATIENT HAS HYPERTENSION. THE DEVICE WAS FORWARDED TO THE MANUFACTURER. NO OTHER MEDICAL ISSUES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2523155 ONYX IMPLANT ONYX DENTAL IMPLANT DZE NORIS MEDICAL LTD NM-G3713 9000271 07290108813104

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown