BEUDAMED
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    MICROCUTTER XCHANGE 30 STAPLER, MICROCUTTER XCHANGE 30 WHITE CARTRIDGE

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

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690117445·Modular Knee Stem Pilot 17mm x 100mm

    BD

    FDA UDI
    PRYOR PRODUCTS·00761887000599·4 LEG, SINGLE POLE, RAKE TOP

    Mariner Outrigger

    FDA UDI
    Seaspine Orthopedics Corporation·10889981179724·Z-Rod, Dia. 6.0mm, Co-Cr, 170mm

    FRIADENT PLUS DENTAL IMPLANT SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Dental

    RAPTOR FACET FIXATION SYSTEM

    FDA 510(k)
    FDA Unclassified ·Unknown

    MAGEC SPINAL BRACING AND DISTRACTION SYSTEM

    FDA Adverse Event
    Injury ·ELLIPSE TECHNOLOGIES, INC.·Product code PGN·June 23, 2014

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·May 31, 2013

    SYNCHRON® SYSTEMS RHEUMATOID FACTOR (RF) REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHR·June 25, 2011

    PUMP MMT-715NAP PRDGM INS V2.1 PL EN

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LZG·August 27, 2008

    SUPERSHEATH

    FDA Adverse Event
    Malfunction ·TOGO MEDIKIT CO. LTD.·Product code DRE·December 2, 2016

    MAGEC SPINAL BRACING AND DISTRACTION SYSTEM

    FDA Adverse Event
    Injury ·ELLIPSE TECHNOLOGIES, INC.·Product code PGN·May 25, 2014

    SUPER SHEATH

    FDA Adverse Event
    Injury ·TOGO MEDIKIT CO., LTD.·Product code DRE·June 2, 2022

    SUPERSHEATH

    FDA Adverse Event
    Injury ·TOGO MEDIKIT CO. LTD.·Product code DRE·August 12, 2018

    SUPERSHEATH

    FDA Adverse Event
    Malfunction ·TOGO MEDIKIT CO. LTD.·Product code DRE·December 11, 2016

    SUPER SHEATH

    FDA Adverse Event
    Injury ·TOGO MEDIKIT CO.LTD.·Product code DRE·January 18, 2018

    MAGEC SPINAL BRACING AND DISTRACTION SYSTEM

    FDA Adverse Event
    Injury ·ELLIPSE TECHNOLOGIES, INC.·Product code PGN·May 21, 2014

    SUPER SHEATH

    FDA Adverse Event
    Injury ·TOGO MEDIKIT CO., LTD.·Product code DRE·March 21, 2023

    SUPER SHEATH

    FDA Adverse Event
    Injury ·TOGO MEDIKIT CO. LTD.·Product code DRE·April 28, 2020

    SUPERSHEATH

    FDA Adverse Event
    Injury ·TOGO MEDIKIT CO. LTD.·Product code DRE·April 11, 2017