BEUDAMED
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    DILATOR, VESSEL & INTRODUCER, SHEATH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517356543·CoRoent Small Interlock Guide, 10mm DTS

    DIO PROTEM IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    SOZO

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TRANSTAR

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FPO·May 6, 2010

    FINELINE II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·October 10, 2012

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 7, 2014

    Promote Quadra, Sterile EO, Model # / Part #: CD3221-36/100025054, 60019195; CD3223-36P/100013763; CD3239-40/100029115, 100029254, 100037181; CD3239-40Q/100029116, 100029244, 100037115

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018