BEUDAMED
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    SIEMENS MULTIVIEW WORKSTATION MODIFICATIONS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EQUINOXE REVERSE 38MM HUMERAL LINER +0

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·August 17, 2022

    ORTHOPILOT 2

    FDA 510(k)
    FDA Class 2 ·Neurology

    PLASMAKINETIC ENDOUROLOGY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    EQUINOXE REVERSE 46MM GLENOSPHERE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·October 2, 2024

    WAVEWRITER ALPHA 16

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·June 2, 2023

    EQUINOXE REVERSE 42MM HUMERAL LINER +2.5

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·August 4, 2023

    EQUINOXE REVERSE TRAY ADAPTER PLATE TRAY +0

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·June 11, 2024

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·March 20, 2020

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·July 3, 2019

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 12, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 2, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

    PRONOVA BLUE MONO POLY(HEXAFLUOROPROPYLENE)SUTURE

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code GAQ·March 27, 2013

    PENTA SURGICAL LEAD

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·March 16, 2011

    CARDIOCAP 5

    FDA Adverse Event
    Malfunction ·GE HEALTHCARE FINLAND OY·Product code MHX·April 2, 2008