BEUDAMED
    FDA Registration Active 🇺🇸 United States

    TRUERELIEF

    Reg #: 3015550326 · FEI: 3015550326 · Expires 2026
    View on FDA
    Products
    1
    Proprietary Names
    7
    Establishment Types
    3
    Classifications
    1

    Registration Details

    Registration Name
    TRUERELIEF
    Registration Number
    3015550326
    FEI Number
    3015550326
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    100 Wilshire Boulevard, Suite 700
    City
    Santa Monica
    State
    CA
    ZIP
    90401
    Country
    US

    Regulatory Submissions

    510(k) Number
    K070474

    Owner / Operator

    Firm Name
    TrueRelief
    Operator Number
    10060510
    Address
    100 Wilshire Boulevard, Suite 700
    City
    Santa Monica
    State
    CA
    Postal Code
    90401
    Country
    US
    Correspondent
    John Crosson

    Products

    Device Name Product Code
    Stimulator, Nerve, Transcutaneous, For Pain Relief GZJ

    Proprietary Names

    TRUERELIEF, Model 1250 TRUERELIEF Device, TRUERELIEF 1250 TRUERELIEF Kit, Model TR1250C TRUERELIEF Kit TRUERELIEF Secondary Probe, Model P12S Secondary Probe TRUERELIEF Power Cord with Wall Wart, Model WW12 Power Cord with Wall Wart TRUERELIEF Primary Probe, Model P12P Primary Probe TRUERELIEF Probe Tips, Probe Tips, Model P12T10 Probe Tips TrueRellief Device

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device