BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Omnilux Revive

    Reg #: 3008776882 · FEI: 3008776882 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    The Lotus Global Group, Inc.
    Registration Number
    3008776882
    FEI Number
    3008776882
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    1290 Jefferson St Ste C
    City
    Napa
    State
    CA
    ZIP
    94559
    Country
    US

    Regulatory Submissions

    510(k) Number
    K030426

    Owner / Operator

    Firm Name
    GlobalMed Technologies Co
    Operator Number
    10051883
    Address
    1290 Jefferson Street, Ste C
    City
    Napa
    State
    CA
    Postal Code
    94559
    Country
    US
    Correspondent
    Sanders Ergas

    Products

    Device Name Product Code
    Powered Laser Surgical Instrument GEX

    Proprietary Names

    Omnilux Revive

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility