BEUDAMED
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    SECURMIX

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CUSTOM PROCEDURE KIT

    FDA UDI
    MEDIVATORS INC.·40677964004108·The ENDO CARRY-ON Procedure Kit contains all of...

    Halyard

    FDA UDI
    Avanos Medical, Inc.·10680651316186·SURGPN,-,CSTMKT,-,OQ,5

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040179338·Diamond Discs

    Smile Spa

    FDA UDI
    Access Dental Lab, LLC·00850007728151·Ultrasonic UV cleaner; smile spa safely cleans:...

    CURE™ ACP

    FDA UDI
    MEDITECH SPINE, LLC·B167700003670·

    Spacelabs Healthcare

    FDA UDI
    SPACELABS HEALTHCARE (WASHINGTON), INC·10841522126215·HOLTER LEADWIRES, EVO/ARIA, RED. 10PK

    Spacelabs Healthcare

    FDA UDI
    SPACELABS HEALTHCARE (WASHINGTON), INC·10841522118432·HOLTER LEADWIRES, EVO/ARIA, RED. 10PK

    FlowLogic Agile

    FDA UDI
    SONENDO, INC.·00810209421120·FlowLogic Agile Shaping File 20 Variable, 31mm

    CURE™ ACP

    FDA UDI
    MEDITECH SPINE, LLC·B167S1700003670·

    SPECTRA-VRM Q-SWITCHED ND:YAG LASER SYSTEM, SPECTRA-VRM

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

    ALKALINE PHOSPHATASE LIQUID REAGENT-KINETIC, MODELS A504-150 AND A504-500H

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·October 4, 2023

    MONARCH PLATFORM

    FDA Adverse Event
    Malfunction ·AURIS HEALTH, INC.·Product code EOQ·September 27, 2022

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·February 22, 2024

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 18, 2023

    LIFEPAK(R) 12 DEFIBRILLATOR/MONITOR SERIES

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·March 12, 2013

    ENDURANT ABDOMINAL STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code MIH·February 18, 2011

    SERVO I

    FDA Adverse Event
    Injury ·MAQUET·Product code CBK·February 15, 2008

    EVIS EXERA III VIDEO SYSTEM CENTER

    FDA Adverse Event
    Injury ·SHIRAKAWA OLYMPUS CO., LTD.·Product code FET·August 18, 2024