BEUDAMED
    FDA Registration Active 🇩🇪 Germany

    OSTEONICS

    Reg #: 9610622 · FEI: 3002807231 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    21
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    STRYKER TRAUMA GMBH
    Registration Number
    9610622
    FEI Number
    3002807231
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    PROF. KUENTSCHER STR. 1-5
    City
    SCHOENKIRCHEN Schleswig-Holstein
    Country
    DE

    Owner / Operator

    Firm Name
    STRYKER CORP.
    Operator Number
    1811755
    Address
    4100 East Milham Ave.
    City
    Kalamazoo
    State
    MI
    Postal Code
    49001
    Country
    US

    Products

    Device Name Product Code
    Screwdriver HXX

    Proprietary Names

    OSTEONICS STRYKER AUTOMATIC SCREWDRIVER SET SCREWDRIVER ORTHOPEDIC SCREWDRIVER Biosteon Wedge Interference Screw System ACL Reconstruction Accessories Universal ACL Instrumentation Bioabsorable Wedge Interference Screw System Cross-Screw System DRIVER; SCREW INSERTER CalcLock Extreme MaxLock Extreme General Instruments Mini Variable MaxTorque DRLock Extreme HexStar Intraosseous Fixation System Mini MaxLock Screwdriver Mini MaxTorque

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)