BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Longeviti Neuro Solutions

    Reg #: 3014680740 · FEI: 3014680740 · Expires 2026
    View on FDA
    Products
    4
    Proprietary Names
    13
    Establishment Types
    2
    Classifications
    4

    Registration Details

    Registration Name
    Longeviti Neuro Solutions
    Registration Number
    3014680740
    FEI Number
    3014680740
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    101 W. Dickman St, Suite 600
    City
    Baltimore
    State
    MD
    ZIP
    21230
    Country
    US

    Regulatory Submissions

    510(k) Number
    K231920

    Owner / Operator

    Firm Name
    Longeviti Neuro Solutions
    Operator Number
    10057995
    Address
    303 International Circle Suite 150
    City
    Hunt Valley
    State
    MD
    Postal Code
    21030
    Country
    US

    Products

    Device Name Product Code
    Plate, Cranioplasty, Preformed, Non-Alterable GXN
    Filler, Bone Void, Non-Alterable Compound For Cranioplasty PJN
    Template HWT
    Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction KKY

    Proprietary Names

    ClearFit OTS Cranial Implant ClearFit ClearFit OTS Longeviti Convenience Kit 1 Longeviti Convenience Kit 4 ClearFit OTS Cover ClearFit OTS Disc ClearFit OTS Hemi ClearFit OTS Chiari Longeviti Convenience Kit 3 Longeviti Convenience Kit 5 Longeviti Convenience Kit 2 InvisiShunt

    Establishment Types

    Manufacture Medical Device Develop Specifications But Do Not Manufacture At This Facility