BEUDAMED
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    SC2000 DIAGNOSTIC ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169373471·BLADE 5102017 20MM WIDE VESSELBLADE 17CM

    RHEAD

    FDA UDI
    Stryker GmbH·00886385024080·Stem Implant 6mm Collar,Size 4

    HEARTWARE® VENTRICULAR ASSIST SYSTEM-CONTROLLER2.0

    FDA Adverse Event
    Malfunction ·HEARTWARE, INC·Product code DSQ·September 14, 2017

    Plateau Spacer System

    FDA UDI
    Life Spine, Inc.·00190837026011·PLATEAU Interbody, Straight, Bulleted, 10mm 20m...

    SPIRA-L

    FDA UDI
    CAMBER SPINE TECHNOLOGIES, LLC·B030SPL1020170·Trial, Bi-Convex, 8° Lordotic, 18 x 60mm, 10mm

    SPIRA®-A Integrated

    FDA UDI
    CAMBER SPINE TECHNOLOGIES, LLC·B030SAZ1020170·SPIRA®-A Integrated,Trial, 24x32mm, 20° Lordoti...

    Plateau Spacer System

    FDA UDI
    Life Spine, Inc.·00190837009762·

    COVERIS

    FDA UDI
    CAMBER SPINE TECHNOLOGIES, LLC·B030CS1020170·Trial, 13 x 18mm, Parallel, 5mm

    SPIRA-O

    FDA UDI
    CAMBER SPINE TECHNOLOGIES, LLC·B030SPO1020170·Trial Bi-Convex 20° Lordotic, 26mm x 28mm, 17mm

    SPIRA-A

    FDA UDI
    CAMBER SPINE TECHNOLOGIES, LLC·B030SPA1020170·Trial, 26 x 32mm, 15° Lordotic, 15mm

    Enza-O

    FDA UDI
    CAMBER SPINE TECHNOLOGIES, LLC·B030EZO1020170·ENZA®-O Trial 30mm x 38mm, 15° Lordotic, 15mm

    SPIRA-C

    FDA UDI
    CAMBER SPINE TECHNOLOGIES, LLC·B030SPC1020170·Trial,15mm x 18mm Lordotic 7°, 5mm

    RHEAD RECON STEM IMPLANT NON-COATED, SIZE 4

    FDA Adverse Event
    Malfunction ·STRYKER GMBH·Product code KWI·December 29, 2015

    VARISEED 7.0

    FDA 510(k)
    FDA Class 2 ·Radiology

    EUROIMMUN HIPPOCAMPUS/CEREBELLUM/GLUTAMATE RECEPTOR/IFA BIOCHIP MOSAIC TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Immunology

    UNKNOWN VLOC PRODUCT

    FDA Adverse Event
    Injury ·COVIDIEN LP LLC NORTH HAVEN·Product code GAM·May 13, 2020

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 9, 2013

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 18, 2011

    ENDEAVOR RESOLUTE RX CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code NIQ·August 7, 2008