BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Omnilux Revive & Blue

    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
    K043329

    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 & Blue

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility