BEUDAMED
    FDA Registration Active 🇺🇸 United States

    NEUROLIEF Inc.

    Reg #: 3019551144 · FEI: 3019551144 · Expires 2026
    View on FDA
    Products
    2
    Proprietary Names
    3
    Establishment Types
    1
    Classifications
    2

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    Registration Details

    Registration Name
    NEUROLIEF Inc.
    Registration Number
    3019551144
    FEI Number
    3019551144
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    Yes
    Address
    10211 W Sample Road #109
    City
    Coral Springs
    State
    FL
    ZIP
    33065
    Country
    US

    Regulatory Submissions

    510(k) Number
    K212106
    PMA Number
    P250010

    Owner / Operator

    Firm Name
    Neurolief
    Operator Number
    10081665
    Address
    12 Giborei Israel
    City
    Netanya
    State
    Central
    Postal Code
    4250412
    Country
    IL
    Correspondent
    Dganit Litinsky

    Products

    Device Name Product Code
    Stimulator, Nerve, Electrical, Transcutaneous, For Migraine PCC
    Cranial Electrotherapy Stimulator To Treat Depression JXK

    Proprietary Names

    Relivion Proliv™Rx System Proliv™Rx external Combined Occipital and Trigeminal Afferent Stimulation (eCOT-AS)

    Establishment Types

    Complaint File Establishment per 21 CFR 820.198