BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SYBRONPRO TL

    MDR report key: 2073430 · Received May 1, 2011

    Report

    Report Number
    2016150-2011-00072
    Event Type
    Injury
    Date Received
    May 1, 2011
    Date of Event
    March 15, 2011
    Report Date
    April 1, 2011
    Manufacturer
    EBI INC.
    Product Code
    DZE
    Adverse Event
    Yes
    Report Source
    Distributor report
    Reporter Location
    NJ, US
    Reporter Occupation
    DENTIST

    Narratives

    Description of Event or Problem · 1

    ON (B)(6), 2011 A DOCTOR REPORTED THAT A PATIENT LOST A SYBRONPRO TL IMPLANT APPROXIMATELY TWO (2) WEEKS AFTER PLACEMENT DUE TO NON-OSSEOINTEGRATION

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SYBRONPRO TL IMPLANT, ENDOSSEOUS, ROOT-FORM DZE EBI INC. 081150

    Patients

    Seq Age Sex Outcome Treatment
    1 49 YR Other| R