BEUDAMED
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    LOCAL PLEXUS BLOCK ANESTHESIA CATHETER KITS

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515230651·Bellucci Wullstein Ret, right, solid blds left

    AIA-PACK BMG

    FDA 510(k)
    FDA Class 2 ·Immunology

    RX ROCKER TRIUMPH, JR. WHEELCHAIR

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    HYDRO THERMABLATOR (HTA) ENDOMETRIAL ABLATION SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code MNB·November 22, 2010

    REJUVENATE STRGHT PRFIT TMZF MOD STEM SIZE 9

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·January 9, 2013

    TELIGEN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 1, 2014

    PM1214 NUANCE SR RF; PM1230 and PM2230 NUANCE MRI; PM2214 NUANCE DR RF These low voltage (LV) devices are implantable pacemaker pulse generators, intended to be permanently implanted in the body, that have a power supply and electronic circuits that produce a periodic electrical pulse to stimulate the heart. These devices are used as a substitute for the heart's intrinsic pacing system to correct both intermittent and continuous cardiac rhythm disorders.

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·October 25, 2017