BEUDAMED
    FDA Adverse Event Other Summary report: N

    IMPLANTIUM

    MDR report key: 1002910 · Received February 22, 2008

    Report

    Report Number
    3004578807-2008-00031
    Event Type
    Other
    Date Received
    February 22, 2008
    Date of Event
    September 22, 2006
    Report Date
    October 12, 2007
    Manufacturer
    DENTIUM CO., LTD.
    Product Code
    DZE
    PMA / PMN Number
    K041368
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KS
    Reporter Occupation
    DENTIST

    Narratives

    Additional Manufacturer Narrative · 1

    ACCORDING TO OUR INVESTIGATION, THERE WAS NO DISCREPANCY ON OUR PRODUCT. CONCLUSION: BASED ON OUR INSPECTION AND TEST RESULTS, THE RETURNED PRODUCT HAS BEEN FOUND TO BE WITHIN SPECIFICATIONS. THEREFORE, THE IMPLANT FAILURE IS MOST LIKELY DUE TO CAUSES OTHER THAN THE PRODUCT SUCH AS SURGICAL MISTAKE, PT BONE CONDITION, PT ORAL HYGIENE, OR PT BEHAVIOR. SEE SCANNED PAGES. SEE SCANNED PAGES.

    Description of Event or Problem · 1

    THE IMPLANT FAILED DUE TO PT HEALTH HABIT AND POOR ORAL HYGIENE. FIXTURE WAS PLACED AT # 27 AND REMOVED AFTER 2 MOS. BONE GRAFT MATERIAL WAS USED. PROSTHETICS ATTACHMENT (BRIDGE). POOR ORAL HYGIENE. POOR BONE CONDITION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 IMPLANTIUM ENDOSSEOUS DENTAL IMPLANT DZE DENTIUM CO., LTD. MF4310 05C17-D

    Patients

    Seq Age Sex Outcome Treatment
    1 65 YR Required Intervention