BEUDAMED
    FDA Registration Active 🇺🇸 United States

    InterX Technologies

    Reg #: 3004786509 · FEI: 3004786509 · Expires 2026
    View on FDA
    Products
    3
    Proprietary Names
    4
    Establishment Types
    2
    Classifications
    3

    Registration Details

    Registration Name
    InterX Technologies
    Registration Number
    3004786509
    FEI Number
    3004786509
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    3465 Technology Dr., Suite A
    City
    Plano
    State
    TX
    ZIP
    75074
    Country
    US

    Regulatory Submissions

    510(k) Number
    K130816

    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
    Electrode, Cutaneous GXY
    Stimulator, Nerve, Transcutaneous, For Pain Relief GZJ
    Stimulator, Transcutaneous Electrical, Aesthetic Purposes NFO

    Proprietary Names

    InterX Self-Adhesive Dual Electrode - Non-Sterile InterX5000 InterX500 Flexible Array Electrode InterX 1000/Derma 200 Stimulator For Cosmetic Use

    Establishment Types

    Repack or Relabel Medical Device Manufacture Medical Device