BEUDAMED
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    FREQUENCY 55 (METHAFILCON A) HYDROPHILIC CONTACT LENS FOR DAILY WEAR

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    artegral HD

    FDA UDI
    Merz Dental GmbH·D7091973063·posteriors; shade B2; size L; lower jaw

    15W CERALAS D 1470NM DIODE LASER

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

    ACIST Kodama Intravascular Ultrasound Catheter, ACIST HDi System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VERSACARE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·June 5, 2014

    ENDURANT ABDOMINAL STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·February 21, 2013

    ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK INSTRUMENT MANUFACTURING·Product code LXH·January 28, 2011

    PROXIMATE I L S INTRALUMINAL STAPLER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GAG·June 17, 1997