BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Luminopia One

    Reg #: 3023855046 · FEI: 3023855046 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    2
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    LUMINOPIA INC
    Registration Number
    3023855046
    FEI Number
    3023855046
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    955 Massachusetts Ave, #335
    City
    Cambridge
    State
    MA
    ZIP
    02139
    Country
    US

    Regulatory Submissions

    510(k) Number
    DEN210005

    Owner / Operator

    Firm Name
    Luminopia Inc
    Operator Number
    10085892
    Address
    955 Massachusetts Ave, #335
    City
    Cambridge
    State
    MA
    Postal Code
    02139
    Country
    US
    Correspondent
    Endri Angjeli

    Products

    Device Name Product Code
    Digital Therapy Device For Amblyopia QQU

    Proprietary Names

    Luminopia One Luminopia

    Establishment Types

    Manufacture Medical Device