BEUDAMED
    FDA Registration Active 🇺🇸 United States

    JBA-FEET LLLT Red and Infrared Light Pain Relief Device for Feet

    Reg #: 3017415521 · FEI: 3017415521 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    9
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    AQP ONE, INC.
    Registration Number
    3017415521
    FEI Number
    3017415521
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    11555 MONARCH STREET
    City
    Garden Grove
    State
    CA
    ZIP
    92841
    Country
    US

    Owner / Operator

    Firm Name
    AQP ONE, INC.
    Operator Number
    10090383
    Address
    11555 MONARCH STREET
    City
    Garden Grove
    State
    CA
    Postal Code
    92841
    Country
    US

    Products

    Device Name Product Code
    Massager, Therapeutic, Electric ISA

    Proprietary Names

    JBA-FEET LLLT Red and Infrared Light Pain Relief Device for Feet JBA-VH LED Gynecological Therapy Device for Vaginal Health JBA-ACU LLLT Pain Relief Device JBA-VPW LLLT Watch for Vessel Restore and Pain Relief with Pads JBA-BELT Red and Infrared Light Pain Relief Belt JBA-SBH LLLT LED Skin Handheld Device JBA-PBH LLLT Pain Relief Handheld Device JBA-VRW LLLT Watch for Vessel Restore – No Pad JBA-HEAD LLLT Red and Infrared Light Cap

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility