BEUDAMED
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    Octa Abutment Driver

    FDA UDI
    Osstem Implant Co., Ltd.·08800000944692·

    Octa Abutment Driver

    FDA UDI
    Osstem Implant Co., Ltd.·08809892360801·

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 25, 2025

    PERMANENT DEFIBRILLATOR ELECTRODES

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL·Product code NVY·August 12, 2023

    ACUVUE® OASYS®

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON VISION CARE, INC. ¿ US·Product code LPM·March 4, 2016

    PACEMAKER

    FDA Adverse Event
    TELECTRONICS PACING SYSTEMS, INC.·Product code DXY·October 26, 1993

    INTRALASE FS1 LASER

    FDA Adverse Event
    Injury ·AMO MANUFACTURING USA, LLC.·Product code HNO·May 26, 2011

    IMPELLA CP

    FDA Adverse Event
    Malfunction ·ABIOMED, INC.·Product code OZD·September 21, 2023

    MATRIXNEURO BURR HOLE COVER F/SHUNT O/DR

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HRS·October 7, 2025

    MATRIXNEURO BURR HOLE COVER F/SHUNT O/DR

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HRS·October 7, 2025

    MATRIXNEURO BURR HOLE COVER F/SHUNT O/DR

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HRS·October 7, 2025

    MEDTRONIC DEFIBRILLATOR

    FDA Adverse Event
    Injury ·Product code LWS·March 19, 2012

    NAVISTAR THERMOCOOL DIAGNOSTIC/ABLATION DEFLECTABLE TIP CATHETER

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code OAD·June 13, 2011

    EVEREST SPINAL SYSTEM

    FDA Adverse Event
    Injury ·K2M, INC.·Product code LXH·October 19, 2017

    LASSO® NAV ECO VARIABLE CATHETER

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code DRF·August 29, 2012

    ACUVUE OASYS®1 DAY WITH HYDRALUXE¿ TECHNOLOGY

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON VISION CARE - IRELAND·Product code LPL·August 18, 2023

    EOPA ARTERIAL CANNULA

    FDA Adverse Event
    Malfunction ·PERFUSION SYSTEMS·Product code DWF·May 29, 2024

    CELL-DYN RUBY SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code GKZ·September 23, 2024

    AIR OPTIX FOR ASTIGMATISM

    FDA Adverse Event
    Injury ·PT. CIBA VISION BATAM·Product code LPL·December 7, 2015

    EKOSONIC ENDOVASCULAR DEVICE, 135X40CM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KRA·March 30, 2022