BEUDAMED
    FDA Adverse Event Injury Summary report: N

    AXIOM PX IMPLANT

    MDR report key: 8825150 · Received July 25, 2019

    Report

    Report Number
    8020776-2019-00696
    Event Type
    Injury
    Date Received
    July 25, 2019
    Date of Event
    March 23, 2019
    Report Date
    July 24, 2019
    Manufacturer
    ANTHOGYR
    Product Code
    DZE
    UDI-DI
    03663394002585
    PMA / PMN Number
    K161177
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CH
    Reporter Occupation
    DENTIST

    Narratives

    Additional Manufacturer Narrative · 1

    ACCORDING TO THE PRACTITIONER THE IMPLANT IS LOST (LOSS OF OSTEOINTEGRATION) AFTER IMPLANT HAS BEEN RESTORED. THE IMPLANT HAS BEEN PLACED IN 37 POSITION ON (B)(6) 2018 AND REMOVED ON (B)(6) 2019. THE IMPLANT HAS FOLLOWED THE COMPLETE MANUFACTURING CYCLE, HAS BEEN VERIFIED AT EACH STAGE OF PRODUCTION, AND HAS BEEN SUBMITTED TO A FINAL RELEASE BEFORE PROVISION OF THE DEVICE ON THE MARKET, WHICH ULTIMATELY GUARANTEES ITS CONFORMITY. THE IMPLANT HAS BEEN EVALUATED THROUGH A BIOLOGICAL RISK ASSESSMENT WHICH CONCLUDES THAT ITS TOXICOLOGICAL PROFILE IS ACCEPTABLE. THE IMPLANT LOSS SUGGESTS THAT THE SOURCE OF THE PROBLEM WAS LIKELY TO COME FROM PROCEDURAL ERRORS AND/OR THE LACK OF OSSEOINTEGRATION. ADDITIONALLY, OTHER FACTORS THAT MAY HAVE CONTRIBUTED TO THE IMPLANT FAILURE INCLUDE BONE CONDITION, PATIENT ORAL HYGIENE, OR PATIENT BEHAVIOR.

    Description of Event or Problem · 1

    IMPLANT IS LOST (LOSS OF OSTEOINTEGRATION) AFTER IMPLANT HAS BEEN RESTORED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    619221 AXIOM PX IMPLANT IMPLANT AXIOM D. 4.0 X 10.0 DZE ANTHOGYR PX40100 18-283762 03663394002585

    Patients

    Seq Age Sex Outcome Treatment
    1 39 YR