BEUDAMED
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    NEWPORT ELECTRONIC MANOMETER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    n/a

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00885074547480·PADDLE SHAVER 2941308 8MM LATERAL

    Cohere

    FDA UDI
    Nuvasive, Inc.·00887517017536·COHERE Pivoting Trial, 14x11x30mm 8°

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471150751·K-WIRE - SINGLE TROCAR 1.25mm DIA x 200mm

    NUTRA LIGHT RED

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

    REMOTENURSE PATIENT MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·April 11, 2014

    IMMAGE® 800 IMMUNOCHEMISTRY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JQX·December 29, 2010

    PINNACLE MTL INS NEUT40IDX60OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·February 4, 2013

    ev3 Pipeline Flex Embolization Device. For neurological endovascular use.

    FDA Enforcement
    Class I ·Terminated·Micro Therapeutics Inc, Dba Ev3 Neurovascular·April 1, 2020