BEUDAMED
    FDA Registration Active 🇫🇷 France

    LUMIS

    Reg #: 3011221483 · FEI: 3011221483 · Expires 2025
    View on FDA
    Products
    4
    Proprietary Names
    4
    Establishment Types
    1
    Classifications
    4

    Registration Details

    Registration Name
    RESCOLL MANUFACTURING
    Registration Number
    3011221483
    FEI Number
    3011221483
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    4 Chemin du Solarium
    City
    Gradignan Nouvelle-Aquitaine
    Country
    FR

    Regulatory Submissions

    510(k) Number
    K133575

    Owner / Operator

    Firm Name
    RESCOLL 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
    Appliance, Fixation, Spinal Interlaminal KWP
    Appliance, Fixation, Spinal Intervertebral Body KWQ
    Orthosis, Spinal Pedicle Fixation MNI
    Orthosis, Spondylolisthesis Spinal Fixation MNH

    Proprietary Names

    LUMIS U.L.I.S ULIS L.U.M.I.S

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)