BEUDAMED
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    MENTOR SELF-CATH PLUS

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

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040062678·Endoflex Hedstrom Files 25 mm

    SCANLAN® Titanium Forceps

    FDA UDI
    SCANLAN INTERNATIONAL INC·00846159003734·S LEGACY Mic fcp, RH NS DG, 1x2 t, str 1.0 mm D...

    THE CARDIAC READER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    VIRIDIS LASER

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

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·January 26, 2012

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·January 26, 2012

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC INC.·Product code KWP·October 15, 2009

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC INC.·Product code KWP·December 31, 2009

    SALINE MAMMARY IMPLANT, 370 CC

    FDA Adverse Event
    MENTOR CORP.·Product code FWM·October 24, 1994

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC INC.·Product code KWP·October 29, 2009

    HEYER-SCHULTE MAMMARY PROSTHESIS, 250 CC

    FDA Adverse Event
    V. MUELLER DIV. BAXTER HEALTHCARE CORP.·Product code FTR·October 24, 1994

    SURGITEK MAMMARY IMPLANT, 300 CC

    FDA Adverse Event
    MEDICAL ENGINEERING CORP.·Product code FTR·October 24, 1994

    PINNACLE MTL INS NEUT36IDX56OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·March 14, 2013

    SYNERGY

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·February 23, 2011

    HAKIM PROGRAMMABLE MICRO VALVE

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC.·Product code JXG·August 12, 2014

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·May 21, 2010

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·May 21, 2010

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC INC.·Product code KWP·August 13, 2010

    PRECISE PRO RX CAROTID STENT SYSTEM

    FDA Adverse Event
    Death ·CORDIS DE MEXICO·Product code NIM·July 26, 2011