BEUDAMED
    FDA Registration Active 🇨🇳 China

    Dynarex 10426

    Reg #: 3012363901 · FEI: 3012363901 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    12
    Establishment Types
    4
    Classifications
    1

    Registration Details

    Registration Name
    Shenzhen Lantise Technology Co., Ltd.
    Registration Number
    3012363901
    FEI Number
    3012363901
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Room 201, No.24 Building, the 3rd Industrial Zone, Langxia Community, Songgang Street, Bao 'an District
    City
    Shenzhen Guangdong
    Country
    CN

    Owner / Operator

    Firm Name
    Shenzhen Lantise Technology Co., Ltd.
    Operator Number
    10055105
    Address
    Room 201, No.24 Building, the 3rd Industrial Zone, Langxia Community, Songgang Street, Bao 'an District
    City
    Shenzhen
    State
    Guangdong
    Postal Code
    518105
    Country
    CN

    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
    Mattress, Flotation Therapy, Non-Powered IKY

    Proprietary Names

    Dynarex 10426 Dynarex 10425 Dynarex 10433 Dynarex 10427 Dynarex 10422 Dynarex 10432 Dynarex 10421 Dynarex 10420 Dynarex 10431 Dynarex 10428 Dynarex 10424 Dynarex 10423

    Establishment Types

    Manufacture Medical Device Remanufacture Medical Device Manufacture Medical Device for Another Party (Contract Manufacturer) Export Device to the United States But Perform No Other Operation on Device