BEUDAMED
    7 results · 26ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    SHERIDAN/HVT,CF, UNCUFFED

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    POLARIS SPECTACLE FRAMES & LENSES

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    aprevo® anterior and lateral lumbar interbody fusion devices, aprevo® transforaminal lumbar interbody fusion devices

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code PHX·December 31, 2024

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·May 20, 2014

    LINOX SMART SD 65/16

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code LWS·October 9, 2012

    BRAVO

    FDA Adverse Event
    Malfunction ·GIVEN IMAGING LTD.·Product code FFT·August 22, 2010