BEUDAMED
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    ARGYLE YANKAUER SUCTION TUBE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Ultraverse® 018

    FDA UDI
    Bard Peripheral Vascular, Inc.·00801741055300·Ultraverse® 018 PTA Balloon Dilatation Catheter...

    Bioplate®

    FDA UDI
    Bioplate, Inc.·M3848130660·Drill Bit, 1.5mm diam., 10mm

    HX-5/6-1 ENDOSCOPIC CLIPPING DEVICE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    CORVIS ST

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    CAPSUREFIX MRI SURESCAN

    FDA Adverse Event
    Malfunction ·MPRI·Product code NVN·October 31, 2012

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 15, 2014

    BRAVO

    FDA Adverse Event
    Malfunction ·GIVEN IMAGING LTD.·Product code FFT·August 15, 2010

    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