BEUDAMED
    8 results · 24ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    STICK SPONGE

    FDA 510(k)
    FDA Unclassified ·Unknown

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867386501·Cortical Screw, 2.7 mm x 12 mm

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867046740·LO-PRO SCRW TM SS 2.7X 12MMCORTEX

    DEXIS CariVu 3-in-1 by KaVo

    FDA 510(k)
    FDA Class 2 ·Dental

    THEKEN SPINE VU EPOD AND VU LPOD SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SYMBIQ SINGLE CHENNEL

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·April 10, 2014

    EON 16-CHANNEL IPG

    FDA Adverse Event
    Malfunction ·ADVANCED NEUROMODULATION SYSTEMS, INC.·Product code LGW·October 13, 2010

    VITROS 5,1 FS CHEMISTRY SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code JJE·December 20, 2012