BEUDAMED
    FDA Registration Active 🇫🇷 France

    LOPITZ MANUFACTURING

    Reg #: 3011221483 · FEI: 3011221483 · Expires 2026
    View on FDA
    Products
    7
    Proprietary Names
    9
    Establishment Types
    1
    Classifications
    7

    Registration Details

    Registration Name
    LOPITZ MANUFACTURING
    Registration Number
    3011221483
    FEI Number
    3011221483
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    4 Chemin du Solarium
    City
    Gradignan Nouvelle-Aquitaine
    Country
    FR

    Owner / Operator

    Firm Name
    LOPITZ MANUFACTURING
    Operator Number
    10047403
    Address
    4 Chemin du solarium
    City
    GRADIGNAN
    State
    Nouvelle-Aquitaine
    Postal Code
    33170
    Country
    FR
    Correspondent
    Patxi DRIEUX

    Products

    Device Name Product Code
    Bone Fixation Cerclage, Sublaminar OWI
    Appliance, Fixation, Spinal Intervertebral Body KWQ
    Appliance, Fixation, Spinal Interlaminal KWP
    Orthosis, Spinal Pedicle Fixation MNI
    Orthosis, Spondylolisthesis Spinal Fixation MNH
    Thoracolumbosacral Pedicle Screw System NKB
    Spinal Vertebral Body Replacement Device MQP

    Proprietary Names

    JAZZ SYSTEM C3 ULIS L.U.M.I.S LUMIS U.L.I.S UNI-THREAD TLIF/ T CAGE PLIF/ P CAGE

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)