BEUDAMED
    FDA Registration Active 🇺🇸 United States

    XTREEM PULSE

    Reg #: 3012470925 · FEI: 3012470925 · Expires 2026
    View on FDA
    Products
    3
    Proprietary Names
    4
    Establishment Types
    2
    Classifications
    3

    Registration Details

    Registration Name
    XTREEM PULSE
    Registration Number
    3012470925
    FEI Number
    3012470925
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    690 Washington St, # 4B
    City
    New York
    State
    NY
    ZIP
    10014
    Country
    US

    Regulatory Submissions

    510(k) Number
    K173483

    Owner / Operator

    Firm Name
    XTREEM PULSE
    Operator Number
    10057865
    Address
    690 Washington Street, 4B
    City
    New York
    State
    NY
    Postal Code
    10014
    Country
    US
    Correspondent
    Andrew Barile

    Products

    Device Name Product Code
    Device, Counter-Pulsating, External DRN
    Stimulator, Transcutaneous Electrical, Aesthetic Purposes NFO
    Light Based Over The Counter Wrinkle Reduction OHS

    Proprietary Names

    Pure Flow PureLift PureLift PRO PureLift Pro Plus

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device