BEUDAMED
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    Spineart SA

    Manufacturer
    🇨🇭 Switzerland

    SPINEART SA

    FDA registration
    SPINEART SA·47 products·🇨🇭 Switzerland

    Spineart Surgical Illuminator

    FDA UDI
    Lumitex, Inc.·00812432021429·

    Spineart Surgical Illuminator

    FDA UDI
    Lumitex, Inc.·00812432021436·

    Spineart Storz Cable Adaptor

    FDA UDI
    Lumitex, Inc.·00812432022945·

    Spineart ACMI Cable Adaptor

    FDA UDI
    Lumitex, Inc.·00812432022938·

    Spineart Wolf Cable Adaptor

    FDA UDI
    Lumitex, Inc.·00812432022396·

    Spineart Olympus Cable Adaptor

    FDA UDI
    Lumitex, Inc.·00812432022921·

    SPINEART Navigation Instrument System

    FDA 510(k)
    FDA Class 2 ·Neurology

    SPINEART Navigation Instrument System

    FDA 510(k)
    FDA Class 2 ·Neurology

    SPINEART Navigation Instrument System

    FDA 510(k)
    FDA Class 2 ·Neurology

    SPINEART Navigation Instrument System

    FDA 510(k)
    FDA Class 2 ·Neurology

    SPINEART Navigation Instrument System

    FDA 510(k)
    FDA Class 2 ·Neurology

    SPINEART Navigation Instrument System

    FDA 510(k)
    FDA Class 2 ·Neurology

    LUMBAR POSTERIOR TI CAGE

    FDA Adverse Event
    Injury ·3D SYSTEM·Product code MAX·August 28, 2023

    Spineart 2.5mm Universal Reusable Light Cable

    FDA UDI
    Lumitex, Inc.·00812432022143·

    SpineArt Bifurcated Universal Fiber Optic Cable

    FDA UDI
    Lumitex, Inc.·00812432022419·

    SPINEART DRILL

    FDA Adverse Event
    Malfunction ·SPINEART SA·Product code HTW·September 26, 2024

    ROMEO 2 INSTRUMENTATION

    FDA Adverse Event
    Malfunction ·SPINEART SA·Product code MNH·October 18, 2021

    SPINEART MIS K-WIRE 1.2 MM LENGTH 450 MM

    FDA Adverse Event
    Malfunction ·SPINEART SA·Product code HTY·July 26, 2013