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

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    STATAK SOFT TISSUE ATTACHMENT DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SENTINEL

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Titan 3 Low Speed Angle Attachments

    FDA 510(k)
    FDA Class 1 ·Dental

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·May 7, 2022

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·October 12, 2022

    OPTEASE VENA CAVA FILTER

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code DTK·February 14, 2013

    ASR UNI FEMORAL IMPL SIZE 53

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·January 7, 2011

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 29, 2014