BEUDAMED
    FDA Registration Active 🇫🇷 France

    SLEEQ AP+

    Reg #: 3009591332 · FEI: 3009591332 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    18
    Establishment Types
    2
    Classifications
    1

    Registration Details

    Registration Name
    THUASNE SAS
    Registration Number
    3009591332
    FEI Number
    3009591332
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    27 rue de la Jomayere
    City
    SAINT ETIENNE Hauts-de-Seine
    Country
    FR

    Owner / Operator

    Firm Name
    Thuasne, LLC
    Operator Number
    9011981
    Address
    120 Osage Ave
    City
    Kansas City
    State
    KS
    Postal Code
    66105
    Country
    US

    US Agent

    Business Name
    Registrar Corp
    Contact Name
    David Lennarz
    Address
    144 Research Drive
    City
    Hampton
    State
    VA
    ZIP
    23666
    Country
    US
    Email
    [email protected]
    Phone
    757 2240177

    Products

    Device Name Product Code
    Orthosis, Lumbo-Sacral IPY

    Proprietary Names

    SLEEQ AP+ Lombaskin Pro BOA Slim Panel XTR BOA w/Chairback SLEEQ AIR APL Lombatech Pro Lombamum SLEEQ AP BOA LP 8 Lombastab SLEEQ AIR AP SLEEQ APL Lombatech BOA SI SLEEQ AIR AP+ Reversa ProMaster SLEEQ ADAPT 639 SLEEQ ADAPT

    Establishment Types

    Manufacture Medical Device Export Device to the United States But Perform No Other Operation on Device