BEUDAMED
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    STERICYCLE SHARPS MANAGEMENT SERVICE REUSABLE SHARPS CONTAINER, 2 GALLON, RED, STERICYCLE SHARPS MANAGEMENT SERVICES REU

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NexxZr™ T / D-100-22-NT-A100-SD

    FDA UDI
    SAGEMAX BIOCERAMICS, INC·00842271112170·

    MEGA PLUS SPINE SYSTEM

    FDA UDI
    BK MEDITECH CO.,LTD.·08809665580078·Rod(CoCr), Ø6.0 x 70mm

    H-Series Loop Electrodes

    FDA UDI
    GYNEX CORPORATION·GYNX1320071·

    RAVINE Lateral Access System

    FDA UDI
    VB Spine LLC·10888857560536·Lateral Access Blade Size 24x130 mm

    GLOVETEX POWDER FREE LATEX EXAMINATION GLOVES, BLUE, NON-STERILE CONTAINS 50 MCGIN OR LESS OF TOTAL WATER EXTRACTABLE PR

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PROLONG, MODELS PL 18040TC, PL18050TGC, PL18100TGC, PL18150TGC,

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    GORE-TEX INTERING STRETCH VASCULAR GRAFT

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES, INC·Product code DSY·May 11, 2007

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC./HUNTINGTON·Product code HQL·May 11, 2007

    ACRYSOF RESTOR

    FDA Adverse Event
    Other ·ALCON LABORATORIES, INC/ HUNTINGTON·Product code HQL·July 12, 2007

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC./HUNTINGTON·Product code HQL·May 11, 2007

    ACRYSOF RESTOR

    FDA Adverse Event
    Other ·ALCON LABORATORIES, INC / HUNTINGTON·Product code HQL·July 12, 2007

    ACRYSOF

    FDA Adverse Event
    Other ·ALCON LABORATORIES, INC /HUNTINGTON·Product code HQL·July 20, 2007

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·July 16, 2007

    ACRYSOF

    FDA Adverse Event
    Other ·ALCON LABORATORIES, INC/ HUNTINGTON·Product code HQL·July 20, 2007

    SIGN I.M. NAIL

    FDA Adverse Event
    Injury ·SURGICAL IMPLANT GENERATION NETWORK (SIGN)·Product code HSB·August 12, 2009

    SYMPHONY

    FDA Adverse Event
    Injury ·ELA MEDICAL S.A.S.·Product code DXY·March 13, 2007

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC./HUNTINGTON·Product code HQL·October 12, 2007

    CABLE TENSIONER

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code LXH·February 18, 2016

    LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER 20 MEDIUM-LARGE TITANIUM LIGA

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code FZP·July 13, 2007