BEUDAMED
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    DUPEL TRANSPORT IONTOPHORESIS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    MaXcess

    FDA UDI
    Nuvasive, Inc.·00887517128034·MAS PLIF Drill, 5.5mm Extended

    LORENZ FIDUCAIL SCREW

    FDA 510(k)
    FDA Class 2 ·Neurology

    AB BELT

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    PRECISION MONTAGE MRI

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·June 21, 2022

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVY·April 22, 2013

    LIMITORR

    FDA Adverse Event
    INTEGRA NEUROSCIENCES PR·Product code JXG·April 14, 2011

    WIRE POST

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS SELZACH·Product code HTY·June 30, 2008

    KYPHON KURVE BONE FILLER DEVICE 13GA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO·Product code KIH·July 14, 2020

    CADD-Solis VIP ambulatory Infusion Pumps, Model 2120 (21-2120, 21-2125, and 21-2127) Indicated for the following uses: Intra-arterial, subcutaneous, intraperitoneal, in close proximity to nerves, into an intraoperative site, epidural space or subarachnoid space. Therapies that require a continuous rate of infusion, intermittent bolus, and/or with patient-controlled demand doses.

    FDA Enforcement
    Class I ·Ongoing·Smiths Medical ASD Inc.·August 14, 2024