BEUDAMED
    FDA Registration Active 🇩🇪 Germany

    TELIX K Implant System

    Reg #: 8010944 · FEI: 3002806545 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    2
    Classifications
    1

    Registration Details

    Registration Name
    BIEDERMANN MOTECH GMBH & Co. KG
    Registration Number
    8010944
    FEI Number
    3002806545
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    BERTA-SUTTNER-STRASSE 23
    City
    VS-SCHWENNINGEN Baden-Wurttemberg
    Country
    DE

    Regulatory Submissions

    510(k) Number
    K170890

    Owner / Operator

    Firm Name
    BIEDERMANN MOTECH GMBH & Co. KG
    Operator Number
    8010944
    Address
    BERTHA-VON-SUTTNER-STRASSE 23, --
    City
    VILLINGEN-SCHWENNINGEN
    State
    Baden-Wurttemberg
    Postal Code
    D-78054
    Country
    DE
    Correspondent
    Gerd - Federle

    US Agent

    Business Name
    MEDAGENT Inc.
    Contact Name
    Franz Menean
    Address
    264 Lafayette Rd Ste 7
    City
    Portsmouth
    State
    NH
    ZIP
    03801
    Country
    US
    Email
    [email protected]
    Phone
    603 5702039

    Products

    Device Name Product Code
    Intervertebral Fusion Device With Bone Graft, Lumbar MAX

    Proprietary Names

    TELIX K Implant System

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device