BEUDAMED
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    TEKNIMED SAS

    FDA registration
    TEKNIMED SAS·14 products·🇫🇷 France

    MINI-MALAX ADAPTED TO HIGH VISCOSITY INJECTION SYSTEM

    FDA Adverse Event
    Malfunction ·TEKNIMED SAS·Product code JDZ·May 19, 2026

    EUROSCREW TCP NG

    FDA Adverse Event
    Injury ·TEKNIMED SAS·Product code MAI·November 22, 2024

    AMPLIFIX 1G

    FDA Adverse Event
    Malfunction ·TEKNIMED SAS·Product code LOD·January 28, 2025

    ARTHROTWIST TCP 8MM L24MM

    FDA Adverse Event
    Malfunction ·TEKNIMED SAS·Product code MAI·January 9, 2025

    INVICTUS

    FDA Adverse Event
    Injury ·TEKNIMED SAS·Product code NDN·November 1, 2023

    AMPLIFIX 1G

    FDA Adverse Event
    Malfunction ·TEKNIMED SAS·Product code MBB·February 11, 2025

    HIGH V+ Spinal Cement System REF T040321K

    FDA Recall
    Open, Classified ·TEKNIMED SAS Zone Industrielle Montredone 11 Rue D Apollo L'Union France·Product code NDN·December 15, 2022

    HIGH V+ Spinal Cement System REF T040321K

    FDA Enforcement
    Class II ·Ongoing·TEKNIMED SAS·February 15, 2023

    CEMENT RESTRICTOR, SIZE 12

    FDA Adverse Event
    Malfunction ·TEKNIMED SA, ZA DE MONTREDON·Product code ---·February 8, 2008

    OsSatura TCP (pure tricalcium phosphate) 3mm granules packaged in glass jars, Part Numbers: 05-6010-050 5cc, 05-6010-100 10cc, 05-6010-150 15cc & 05-6010-300 30cc

    FDA Recall
    Terminated ·Teknimed SA 11 Rue Apollo L France·Product code MQV·August 31, 2006