BEUDAMED
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    DYONICS VISION 337 AUTOCLAVABLE CAMERA HEAD MODEL 7209048; DYONICS AUTOCLAVABLE CAMERA COUPLER MODEL 7207905

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

    Premier Composite Instruments

    FDA UDI
    PREMIER DENTAL PRODUCTS COMPANY·00348783009767·CPF DE_3

    Inclusive

    FDA UDI
    Preat Corporation·00842092122372·Multi-Unit Abutment Plastic Coping

    SCANLAN® Titanium Forceps

    FDA UDI
    SCANLAN INTERNATIONAL INC·00846159003499·Dennis Micro Forceps, RH, straight DD platform ...

    QUASAR

    FDA UDI
    Modus Medical Devices Inc·G34350037100·MRgRT Insight - Laser Target

    N/A

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613327542332·Ortho Guidance Express Knee Software

    N/A

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613327542363·Ortho Guidance Express Knee Enable

    MD 10, SEM, SM 12, CBM

    FDA 510(k)
    FDA Class 1 ·Dental

    MODIFICATION TO SYNTHES (USA) TROCHANTER STABILIZATION PLATE (TSB) FOR DHS (LINE EXTENSION)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RESPIRATORY HUMIDIFIER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE, LTD.·Product code BTT·December 18, 2009

    RESPIRATORY HUMIDIFIER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE, LTD.·Product code BTT·May 17, 2010

    RESPIRATORY HUMIDIFIER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE, LTD.·Product code BTT·December 18, 2009

    RESPIRATORY HUMIDIFIER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE, LTD.·Product code BTT·November 17, 2009

    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

    VERTEX RECONSTRUCTION SYSTEM

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

    LIGASURE ADVANCE PISTOL GRIP

    FDA Adverse Event
    Malfunction ·COVIDIEN LP·Product code GEI·February 11, 2013

    VASOVIEW HEMOPRO EVH SYSTEM

    FDA Adverse Event
    Injury ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·February 23, 2011