BEUDAMED
    FDA Registration Active 🇬🇧 United Kingdom

    OKULO LIMITED

    Reg #: 3038131813 · FEI: 3038131813 · Expires 2026
    View on FDA
    Products
    2
    Proprietary Names
    1
    Establishment Types
    2
    Classifications
    2

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    Registration Details

    Registration Name
    OKULO LIMITED
    Registration Number
    3038131813
    FEI Number
    3038131813
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    17-19 Berkeley Square,
    City
    Bristol, UK, Bristol, City of
    Country
    GB

    Owner / Operator

    Firm Name
    OKKO Health Inc.
    Operator Number
    10093091
    Address
    131 Continental Dr, Suite 305
    City
    Newark
    State
    DE
    Postal Code
    19713
    Country
    US
    Correspondent
    Stephanie Campbell

    US Agent

    Business Name
    OKKO Health Inc. (USA)
    Contact Name
    Stephanie Campbell
    Address
    131 Continental Dr, Suite 305
    City
    Newark
    State
    DE
    ZIP
    19713
    Country
    US
    Email
    [email protected]
    Phone
    801 6733973

    Products

    Device Name Product Code
    Digital Visual Acuity Test QTO
    Digital Amsler Grid QTW

    Proprietary Names

    OKKO Health App

    Establishment Types

    Manufacture Medical Device Complaint File Establishment per 21 CFR 820.198