BEUDAMED
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    P.F.C. CRUCIATE RETAINING KNEE SYSTEM (SIZE 1.5)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295239833·UNIVERSAL REVISION FEMORAL BROACH 40mm

    PULSERA

    FDA 510(k)
    FDA Class 2 ·Radiology

    syngo®.via protoNeo (Version VA10A)

    FDA 510(k)
    FDA Class 2 ·Radiology

    SYNERGEYES HYBRID CONTACT LENS

    FDA Adverse Event
    Injury ·SYNERGEYES·Product code HQD·June 16, 2014

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·PURITAN BENNETT CORP.·Product code CBK·December 28, 2010

    OBTRYX SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·February 14, 2013

    SEE H10

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDG·June 4, 2018