BEUDAMED
    FDA Registration Active 🇩🇪 Germany

    Percusys

    Reg #: 3005083075 · FEI: 3005083075 · Expires 2025
    View on FDA
    Products
    3
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    3

    Registration Details

    Registration Name
    JOIMAX GMBH
    Registration Number
    3005083075
    FEI Number
    3005083075
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    AMALIENBADSTRASSE 41, Raumfabrik 61
    City
    KARLSRUHE Baden-Wurttemberg
    Country
    DE

    Regulatory Submissions

    510(k) Number
    K143200

    Owner / Operator

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

    US Agent

    Business Name
    GSM Services
    Contact Name
    Gary Mocnik
    Address
    49 Coastal Oak
    City
    Aliso Viejo
    State
    CA
    ZIP
    92656
    Country
    US
    Email
    [email protected]
    Phone
    949 4330413

    Products

    Device Name Product Code
    Thoracolumbosacral Pedicle Screw System NKB
    Orthosis, Spondylolisthesis Spinal Fixation MNH
    Orthosis, Spinal Pedicle Fixation MNI

    Proprietary Names

    Percusys

    Establishment Types

    Repack or Relabel Medical Device