BEUDAMED
    FDA Registration Active 🇮🇪 Ireland

    Lenire

    Reg #: 3018030059 · FEI: 3018030059 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    3
    Classifications
    1

    Registration Details

    Registration Name
    NEUROMOD DEVICES LIMITED
    Registration Number
    3018030059
    FEI Number
    3018030059
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Rainsford Street
    City
    Dublin Dublin (City)
    Country
    IE

    Regulatory Submissions

    510(k) Number
    DEN210033

    Owner / Operator

    Firm Name
    Neuromod Devices Limited
    Operator Number
    10087563
    Address
    Rainsford Street
    City
    Dublin
    State
    Dublin (City)
    Postal Code
    D08 R2YP
    Country
    IE
    Correspondent
    Fran Coogan

    Products

    Device Name Product Code
    Combined Acoustic And Electrical External Stimulation Device For The Relief Of Tinnitus QVN

    Proprietary Names

    Lenire

    Establishment Types

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