BEUDAMED
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    ACUITY BREAK-AWAY GUIDE CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EECP THERAPY SYSTEM, MODEL TS3

    FDA Adverse Event
    Injury ·VASOMEDICAL, INC.·Product code DRN·December 30, 2002

    MINIBLASTER

    FDA 510(k)
    FDA Class 2 ·Dental

    ELECSYS CA 125 II CALSET

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    GRANUFLO

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·May 1, 2013

    UNKNOWN_RECONSTRUCTIVE_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·September 16, 2014

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUCNOS·Product code LKK·May 16, 2011