BEUDAMED
    FDA Adverse Event Injury Summary report: N

    RESTORE 3.75X13 SELF-TAP

    MDR report key: 39054 · Received September 23, 1996

    Report

    Report Number
    2184002-1996-00189
    Event Type
    Injury
    Date Received
    September 23, 1996
    Date of Event
    August 26, 1996
    Report Date
    October 8, 1996
    Manufacturer
    LIFECORE BIOMEDICAL, INC.
    Product Code
    DZE
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    DENTIST

    Narratives

    Description of Event or Problem · 1

    IMPLANT FAILED. EXACT DATE OF OCCURRENCE UNKNOWN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RESTORE 3.75X13 SELF-TAP Implant ENDOSSEOUS IMPLANT DZE LIFECORE BIOMEDICAL, INC. R9005-38-13 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Required Intervention