BEUDAMED
    FDA Registration Active 🇺🇸 United States

    InterX 1000/Derma 200 Stimulator For Cosmetic Use

    Reg #: 3004786509 · FEI: 3004786509 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    1
    Establishment Types
    2
    Classifications
    2

    Registration Details

    Registration Name
    InterX Technologies
    Registration Number
    3004786509
    FEI Number
    3004786509
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    3465 Technology Dr., Suite A
    City
    Plano
    State
    TX
    ZIP
    75074
    Country
    US

    Regulatory Submissions

    510(k) Number
    K070217

    Owner / Operator

    Firm Name
    InterX Technologies
    Operator Number
    10051305
    Address
    3465 Technology Dr., Suite A
    City
    Plano
    State
    TX
    Postal Code
    75074
    Country
    US

    Products

    Device Name Product Code
    Stimulator, Transcutaneous Electrical, Aesthetic Purposes NFO
    Electrode, Cutaneous GXY

    Proprietary Names

    InterX 1000/Derma 200 Stimulator For Cosmetic Use

    Establishment Types

    Repack or Relabel Medical Device Manufacture Medical Device