BEUDAMED
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    KERATIN PRIMARY ANTIBODY

    FDA 510(k)
    FDA Class 2 ·Immunology

    3M™ ESPE™

    FDA UDI
    3M COMPANY·30605861030718·3M™ ESPE™ Gold Anodized Crown Refills, First Mo...

    VARIAX

    FDA UDI
    Stryker GmbH·07613327125924·Core Tray T10 Screw Drawer Clip

    ORTHALIGN PLUS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    SMITH AND NEPHEW TITANIUM INTERFERENCE SCREWS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HEARTMATE II LVAS, EUROPE

    FDA Adverse Event
    Injury ·THORATEC CORP.·Product code DSQ·June 19, 2014

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    UNKNOWN·Product code ITJ·February 2, 2013

    TUBE, GASTROINTESTINAL (AND ACCESS)

    FDA Adverse Event
    Injury ·C. R. BARD INC. (BASD)·Product code KGC·December 20, 2010

    Captus 4000e Thyroid Uptake System, Model Numbers 5430-30151 and 5430-30152 - Product Usage: is intended to be used by trained nuclear Medicine Technologists or Nuclear Medicine Physicians to perform Thyroid Uptake Procedures.

    FDA Enforcement
    Class II ·Terminated·Capintec Inc·April 1, 2020