BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    JOHNSON & JOHNSON STAINING REMOVING COMPOUND

    FDA 510(k)
    FDA Class 1 ·Dental

    FLAME PHOTOMETERS

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    B-1000

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PIPELINE EMBOLIZATION DEVICE

    FDA Adverse Event
    Injury ·EV3 NEUROVASCULAR·Product code OUT·June 10, 2014

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVY·October 11, 2010

    4.5MM LCP® PROXIMAL FEMUR PLATE 6 HOLES/211MM-LEFT

    FDA Adverse Event
    Injury ·SYNTHES·Product code HRS·December 10, 2012

    OPTETRAK Comprehensive Knee System including OPTETRAK RBK PS Tibial Components. NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·October 13, 2021