BEUDAMED
    FDA Registration Active 🇺🇸 United States

    EndoLIF(R) DoubleWedge-Cage

    Reg #: 3005042595 · FEI: 3005042595 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    2
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    JOIMAX, INC.
    Registration Number
    3005042595
    FEI Number
    3005042595
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    140 Technology Drive, Suite 150
    City
    Irvine
    State
    CA
    ZIP
    92618
    Country
    US

    Regulatory Submissions

    510(k) Number
    K203014

    Owner / Operator

    Firm Name
    Joimax GmbH
    Operator Number
    9070895
    Address
    Amalienbadstrasse 41, RaumFabrik 61
    City
    Karlsruhe
    State
    Baden-Wurttemberg
    Postal Code
    76227
    Country
    DE

    Products

    Device Name Product Code
    Intervertebral Fusion Device With Bone Graft, Lumbar MAX

    Proprietary Names

    EndoLIF(R) DoubleWedge-Cage EndoLIF(R) Delta-Cage

    Establishment Types

    Complaint File Establishment per 21 CFR 820.198