BEUDAMED
    FDA Adverse Event Injury Summary report: N

    TI TITAMAX IMPLANT (4.1)4.0X17

    MDR report key: 7012610 · Received November 9, 2017

    Report

    Report Number
    3008261720-2017-00262
    Event Type
    Injury
    Date Received
    November 9, 2017
    Date of Event
    October 19, 2010
    Report Date
    August 14, 2015
    Manufacturer
    NEODENT - JJGC S.A.
    Product Code
    DZE
    UDI-DI
    07898237567037
    PMA / PMN Number
    K101207
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    BR
    Reporter Occupation
    DENTIST

    Narratives

    Additional Manufacturer Narrative · 0

    EXEMPTION NUMBER: E2015015. INSTRADENT USA, INC IS SUBMITTING THE REPORT ON BEHALF OF NEODENT - JJGC.

    Description of Event or Problem · 0

    OS 111551 - THE DENTIST REPORTED THAT ALMOST SIX MONTHS AFTER THE DENTAL IMPLANT WAS INSTALLED IN PATIENT'S MOUTH, IT WAS VERIFIED ITS NON-OSSEOINTEGRATION. PATIENT PRESENTED BONE TYPE III.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    793570 TI TITAMAX IMPLANT (4.1)4.0X17 ENDOSSEOUS DENTAL IMPLANT DZE NEODENT - JJGC S.A. 07898237567037

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention