BEUDAMED
    6 results · 28ms · Sources: EU EUDAMED, US FDA

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    DISPOSABLE HYDROGEL DEFIBRILLATION ELECTRODE/PAD

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    InMode System MiniFX Handpiece

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

    ENDOFAST RELIANT SYSTEM

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

    LENSX LASER SYSTEM

    FDA Adverse Event
    Injury ·ALCON - LENSX LASERS, INC.·Product code OOE·February 8, 2013

    REPLY

    FDA Adverse Event
    Malfunction ·SORIN BIOMEDICA CRM S.R.L.·Product code NVZ·December 15, 2010

    GRANUFLO

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·July 15, 2014