BEUDAMED
    FDA Registration Active 🇮🇱 Israel

    NEUROLIEF Ltd.

    Reg #: 3015088397 · FEI: 3015088397 · Expires 2026
    View on FDA
    Products
    2
    Proprietary Names
    3
    Establishment Types
    3
    Classifications
    2

    Registration Details

    Registration Name
    NEUROLIEF Ltd.
    Registration Number
    3015088397
    FEI Number
    3015088397
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    12 Giborei Israel
    City
    Netanya Central
    Country
    IL

    Regulatory Submissions

    510(k) Number
    K203419
    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

    US Agent

    Business Name
    Neurolief Inc.
    Contact Name
    Lewis Steve Beller
    Address
    10211 W Sample Rd Ste 217
    City
    Coral Springs
    State
    FL
    ZIP
    33065
    Country
    US
    Email
    [email protected]
    Phone
    210 8436778

    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

    Manufacture Medical Device Export Device to the United States But Perform No Other Operation on Device Complaint File Establishment per 21 CFR 820.198