BEUDAMED
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    PROCLEAR COMPATIBLES DAILY WEAR CONTACT LENS

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    artegral

    FDA UDI
    Merz Dental GmbH·D7091970095·anteriors; shade A3.5; mould BOM

    Vial2Bag Direct Connect

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TRIATHLON TS KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PRESTIGE ATRA GRASPERSGL-ACT5MM 36CM

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW ENDOSCOPY·Product code GCJ·April 28, 2014

    DEPUY ASR XL FEM IMP SIZE 47

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·February 20, 2013

    INFINITI VISION SYSTEM OZIL

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·January 14, 2011