BEUDAMED
    FDA Registration Active 🇨🇳 China

    Lens, non-custom(prescription)

    Reg #: 3023010371 · FEI: 3023010371 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    2
    Classifications
    1

    Registration Details

    Registration Name
    SHENZHEN MONI TECHNOLOGY CO.,LTD
    Registration Number
    3023010371
    FEI Number
    3023010371
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    201-1, No.93, Aoer New Village, Baoan Community, Yuanshan Street, Longgang District
    City
    Shenzhen Guangdong
    Country
    CN

    Owner / Operator

    Firm Name
    ShenZhen Moni Technology Co.,Ltd
    Operator Number
    10086630
    Address
    201-1, No.93, Aoer New Village, Baoan Community, Yuanshan Street, Longgang District
    City
    Shenzhen
    State
    Guangdong
    Postal Code
    518115
    Country
    CN
    Correspondent
    Jennifer Qu

    US Agent

    Business Name
    Regrek LLC
    Contact Name
    Leeyeo Kee
    Address
    19 Holly Cove Ln.
    City
    Dover
    State
    DE
    ZIP
    19901
    Country
    US
    Email
    [email protected]
    Phone
    302 6089028

    Products

    Device Name Product Code
    Lens, Spectacle, Non-Custom (Prescription) HQG

    Proprietary Names

    Lens, non-custom(prescription)

    Establishment Types

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