BEUDAMED
    8 results · 26ms · Sources: EU EUDAMED, US FDA

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    POLARIS

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Dental Implant System

    FDA 510(k)
    FDA Class 2 ·Dental

    REFIX INTERNAL FRACTURE FIXATION SCREWS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SOLETRA

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code MHY·December 14, 2010

    XACT CAROTID STENT SYSTEM

    FDA Adverse Event
    Death ·AV-TEMECULA-CT·Product code NIM·February 8, 2013

    PRESIDIO 10 - CERECYTE MICROCOIL

    FDA Adverse Event
    Malfunction ·MICRUS ENDOVASCULAR, LLC·Product code HCG·July 22, 2014

    LARGE EX-FIX 11MM CRBN FBR ROD 250MM / MR-CONDITIONAL

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code KTT·April 12, 2018

    LARGE EX-FIX 11MM CRBN FBR ROD 300MM / MR-CONDITIONAL

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code KTT·April 12, 2018