BEUDAMED
    9 results · 28ms · Sources: EU EUDAMED, US FDA

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    APTUS Cannulated Compression Screws Line Extension, APTUS K-Wire System Line Extension

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VISION XR

    FDA UDI
    BENCO DENTAL SUPPLY CO.·00366975024862·Vision XR Double FB-57 F-Speed Box of 150

    APTIMA COMBO 2 ASSAY (PANTHER SYSTEM)

    FDA 510(k)
    FDA Class 2 ·Microbiology

    IMMUNETECH TOTAL IGE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Immunology

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·September 11, 2024

    ASR ACETABULAR CUPS 50

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·November 13, 2008

    UNKNOWN DEPUY ASR HEAD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KXA·August 18, 2011

    BARD FLAT MESH

    FDA Adverse Event
    Injury ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·July 8, 2013

    ACCOLADE DR SL MRI (Model L311)

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025