BEUDAMED
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    Unicare (K-UNICARE-USA)

    FDA 510(k)
    FDA Class 2 ·Neurology

    Symmetry Surgical

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482001394·Symmetry® Curette, Spinal, Angled, Size 0, 8 in...

    Intrigue

    FDA UDI
    LANCER ORTHODONTICS, INC.·00817573021017·INTRG WHISP ROTH CUS -11T +5A 018 LR

    ANSPACH XMAX, EMAX2 AND EMAX2 PLUS SYSTEM WITH OTOLOGIC ATTACHMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    SELECTIVE MED COMPONENTS, INC. BUFFERED IONTOPHORESIS DRUG DELIVERY SYSTEM ELECTRODES, MODELS I20, I30, I40, I50, AND I7

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    AUTOMATIC ENDOSCOPE REPROCESSOR

    FDA Adverse Event
    Malfunction ·MINNTECH CORP.·Product code NVE·October 30, 2008

    HEARTSTART MRX -EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE - ANDOVER·Product code MKJ·July 20, 2011

    PLUMSET CLAVE PORT CLAVE SITE 103IN NDHP

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·July 12, 2013

    ULTRAPRO MESH UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·April 22, 2021

    PROLENE POLYPROPYLENE MESH UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·April 22, 2021