BEUDAMED
    6 results · 44ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    VITAL MIS PEDICLE SCREW SYSTEM

    FDA Adverse Event
    Injury ·HIGHRIDGE MEDICAL, LLC·Product code NKB·February 24, 2026

    VERTEBRAL BODY TETHERING SYSTEM THE TETHER

    FDA Adverse Event
    Injury ·ZIMVIE / HIGHRIDGE MEDICAL LLC.·Product code QHP·October 28, 2024

    LANX SPINAL FIXATION SCREWS

    FDA Adverse Event
    Injury ·LANX / HIGHRIDGE MEDICAL, LLC.·Product code NKB·November 4, 2024

    LANX PEEK INTERVERTEBRAL BODY FUSION DEVICE

    FDA Adverse Event
    Injury ·LANX / HIGHRIDGE MEDICAL, LLC.·Product code MAX·November 4, 2024

    ORTHOPAK NON-INVASIVE BONE GROWTH STIMULATOR

    FDA Adverse Event
    Malfunction ·HIGHRIDGE MEDICAL, LLC. / ZIMMER BIOMET·Product code LOF·September 19, 2024

    BIOMET SPINAL FIXATION SCREWS

    FDA Adverse Event
    Injury ·BIOME SPINE / HIGHRIDGE MEDICAL, LLC.·Product code NKB·November 4, 2024