BEUDAMED
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    NATURAL-KNEE II POSTERIOR STABILIZED (P.S.) CONDYLAR KNEE TIBIAL INSERTS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Polystar Selection EDITION HD

    FDA UDI
    Merz Dental GmbH·D7091983153·posteriors; shade BL4; size XL; lower jaw

    Microwave Ablation System

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

    ACTIFLO INDWELLING BOWEL CATHETER SYSTEM KIT, MODELS: 32004, 32005, 32006, 32007

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

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·February 28, 2013

    ASR UNI FEMORAL IMPL SIZE 43

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·January 31, 2011

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR PURITAN·Product code CBK·July 3, 2014