BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CM DRIVE IMPLANT 3.5X11.5

    MDR report key: 8372126 · Received February 26, 2019

    Report

    Report Number
    3008261720-2019-00814
    Event Type
    Injury
    Date Received
    February 26, 2019
    Date of Event
    December 19, 2018
    Report Date
    February 26, 2019
    Manufacturer
    NEODENT - JJGC S.A.
    Product Code
    DZE
    UDI-DI
    07899878023319
    PMA / PMN Number
    K123022
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NJ, US
    Reporter Occupation
    DENTIST

    Narratives

    Additional Manufacturer Narrative · 0

    ADDITIONAL PATIENT CODE (DESCRIPTION) IN F10: 1690/ABSCESS. EXEMPTION NUMBER: E2015015. INSTRADENT USA, INC IS SUBMITTING THE REPORT ON BEHALF OF NEODENT - JJGC

    Additional Manufacturer Narrative · 0

    ADDITIONAL PATIENT CODE (DESCRIPTION) IN F10: 1690/ABSCESS. EXEMPTION NUMBER: E2015015. INSTRADENT USA, INC IS SUBMITTING THE REPORT ON BEHALF OF NEODENT - JJGC. AFTER THE EVALUATION WAS NOTICED THAT THE ITEM RECEIVED IS DIFFERENT FROM THE ITEM REPORTED. THEREFORE, THE ITEM WAS CORRECTED AND THE LOT NUMBER WAS NOT CONSIDERED.THE INVESTIGATION OF THE COMPLAINT WAS CARRIED OUT CONSIDERING THE ANALYSIS OF THE INFORMATION GIVEN BY THE DENTIST IN THE GUARANTEE FORM AND VISUAL CONFERENCE OF THE PRODUCT RETURNED BY THE DENTIST.

    Description of Event or Problem · 0

    THE CLINICIAN REPORTED THAT 2.5 MONTHS AFTER THE DENTAL IMPLANT AND HEALING ABUTMENT WERE PLACED IN ADA SITE 9 IN THE MOUTH, THE IMPLANT DID NOT ACHIEVE OSSEOINTEGRATION. CLINICIAN NOTED THE PATIENT'S PAIN, BLEEDING AND ABSCESS. THE PRODUCT WILL BE FORWARDED TO THE MANUFACTURER FOR INVESTIGATION. THERE WERE NO REPORTED POST-OPERATIVE COMPLICATIONS.

    Description of Event or Problem · 0

    THE CLINICIAN REPORTED THAT 2.5 MONTHS AFTER THE DENTAL IMPLANT AND HEALING ABUTMENT WERE PLACED IN ADA SITE 9 IN THE MOUTH, THE IMPLANT DID NOT ACHIEVE OSSEOINTEGRATION. CLINICIAN NOTED THE PATIENT'S PAIN, BLEEDING AND ABSCESS. THE PRODUCT WILL BE FORWARDED TO THE MANUFACTURER FOR INVESTIGATION. THERE WERE NO REPORTED POST-OPERATIVE COMPLICATIONS. (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    162518 CM DRIVE IMPLANT 3.5X11.5 ENDOSSEOUS DENTAL IMPLANT DZE NEODENT - JJGC S.A. 800327604I 07899878023319

    Patients

    Seq Age Sex Outcome Treatment
    1 66 YR Required Intervention HEALING ABUTMENT PLACEMENT| HEALING ABUTMENT PLACEMENT