BEUDAMED
    FDA Registration Active 🇫🇷 France

    Kinetec Maestra

    Reg #: 8020836 · FEI: 3006734242 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    16
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Kinetec SAS
    Registration Number
    8020836
    FEI Number
    3006734242
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Zone Industrielle de Tournes, Rue Maurice Périn
    City
    Tournes Ardennes
    Country
    FR

    Owner / Operator

    Firm Name
    Kinetec USA, Inc.
    Operator Number
    10045573
    Address
    N174W21475 Alcan Drive
    City
    Jackson
    State
    WI
    Postal Code
    53037
    Country
    US
    Correspondent
    Lori Kalsow

    US Agent

    Business Name
    Kinetec USA, Inc.
    Contact Name
    Lori Kalsow
    Address
    N174W21475 Alcan Drive
    City
    Jackson
    State
    WI
    ZIP
    53037
    Country
    US
    Email
    [email protected]
    Phone
    262 6771248 ext. 109

    Products

    Device Name Product Code
    Exerciser, Non-Measuring ION

    Proprietary Names

    Kinetec Maestra Kinetec Centura B&W Kinetec Spectra XL Kinetec Spectra Kinetec Prima XL Kinetec Breva Kinetec Spectra Essential Kinetec Kinetec Centura Lite Kinetec USA Kinetec Performa Kinetec 6080 Kinetec Prima Advance Kinetec Centura Kinetec Centura Elbow Module Kinetec Kompanion

    Establishment Types

    Manufacture Medical Device