BEUDAMED
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    IonicRF Generator

    FDA 510(k)
    FDA Class 2 ·Neurology

    Blade Handle

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112366·CHUCK HANDLE #3K 10CM LONG

    Osteomed

    FDA UDI
    Provision·B504OM32016100·

    Osteomed

    FDA UDI
    Provision·00810041631404·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694032230·1.0mm Drill, Quick Release

    Ophthlamic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·10841668112424·DISPOSABLE BARRAQUER SPECULUM BOX OF 10

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450546109·

    ABSORBENT PAPER POINTS

    FDA UDI
    DiaDent Group International·08806383554480·"An absorbent paper points is an endodontic pap...

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694073264·HPS 1.0mm Drill, Quick Release Sterile Qty 2

    Customized Contour Implant

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

    QAB2A IGM ELISA KIT HRP

    FDA 510(k)
    FDA Class 2 ·Immunology

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·September 13, 2016

    HEARTWARE VENTRICULAR ASSIST SYSTEM - CONTROLLER 2.0

    FDA Adverse Event
    Malfunction ·HEARTWARE, INC.·Product code DSQ·February 28, 2018

    HEARTWARE VENTRICULAR ASSIST SYSTEM-BATTERY

    FDA Adverse Event
    Malfunction ·HEARTWARE, INC.·Product code DSQ·June 7, 2018

    TRUETRACK

    FDA Adverse Event
    Malfunction ·NIPRO DIAGNOSTICS, INC.·Product code NBW·March 1, 2016

    HEARTWARE VENTRICULAR ASSIST SYSTEM - CONTROLLER 2.0

    FDA Adverse Event
    Malfunction ·HEARTWARE, INC.·Product code DSQ·July 16, 2018

    BD VACUTAINER® SST¿ BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·April 30, 2018

    TRUETRACK

    FDA Adverse Event
    Malfunction ·TRIVIDIA HEALTH, INC.·Product code NBW·March 21, 2016

    SOLUS BILIARY STENT AND INTRODUCER SET

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FGE·June 11, 2021

    LPS CEM FEM STEM 12X150MM BOW

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·July 9, 2015