BEUDAMED
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    VAXIOM FAMILY OF RF LESION PROBES & ELEC

    FDA 510(k)
    FDA Class 2 ·Neurology

    ACUMED

    FDA UDI
    Acumed LLC·10806378091285·4.5mm Cannulated Drill, QC

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450180488·

    PRECISION RXI ANALOG AND DIGITAL X-RAY SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Radiology

    SkinPen Precision System

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    BD DISCARDIT¿ II SYRINGE W/O NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·September 25, 2018

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE·Product code KDJ·May 9, 2014

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code IOR·October 23, 2012

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·September 6, 2007

    BD DISCARDIT¿ II 20 ML SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·April 9, 2019

    GLOBAL UNITE STD STEM SZ 12 Product Code: 110012100

    FDA Enforcement
    Class II ·Terminated·DePuy Orthopaedics, Inc.·January 19, 2022

    ACUSON Sequoia Ultrasound Imaging System with Software Version VA25A/B

    FDA Enforcement
    Class II ·Ongoing·Siemens Medical Solutions USA, Inc.·February 9, 2022