BEUDAMED
    FDA Registration Active 🇩🇪 Germany

    K-Wire

    Reg #: 3014314623 · FEI: 3014314623 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    10
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Aristotech Industries GmbH
    Registration Number
    3014314623
    FEI Number
    3014314623
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Alt-Lankwitz 102
    City
    Berlin
    Country
    DE

    Owner / Operator

    Firm Name
    Aristotech Industries GmbH
    Operator Number
    10053573
    Address
    Im Biotechnologiepark
    City
    Luckenwalde
    State
    Brandenburg
    Postal Code
    14943
    Country
    DE
    Correspondent
    Jens-Erik Wegner

    Products

    Device Name Product Code
    Guide, Surgical, Instrument FZX

    Proprietary Names

    K-Wire OsteoBridge Drill Sleeve MetaFix" I Drill Guide PediatrOS" FlexTack"/RigidTack" Target device OsteoBridge" IKA Nail Guiding Impacting/Instrument OsteoBridge" IKA Knee Arthrodesis Guiding Pin Tissue Protector OsteoBridge" Drill Sleeve Double Drill Sleeve OsteoBridge" Protection Sleeve

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)