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    LF900

    FDA UDI
    DAESUNG MAREF CO.,LTD.·08809315677486·Main device 1ea, OVERLAPPING LEG SLEEVE Medium ...

    LF400

    FDA UDI
    DAESUNG MAREF CO.,LTD.·08809802640283·Main device 1ea, OVERLAPPING LEG SLEEVE Medium ...

    LF900

    FDA UDI
    DAESUNG MAREF CO.,LTD.·08809802644571·Main device 1ea, OVERLAPPING LEG SLEEVE Medium ...

    LF900

    FDA UDI
    DAESUNG MAREF CO.,LTD.·08809802643376·Device 1ea , MXW401 2ea , Double hose 1ea, Sing...

    ONX ASCENDING AORTIC 19

    FDA Adverse Event
    Injury ·ON-X LIFE TECHNOLOGIES, INC.·Product code LWQ·August 20, 2021

    DeltaVision OMX SR Imaging System Model Number: 29115476 The DeltaVision OMX SR Imaging System is a piece of laboratory equipment for super resolution imaging offluorescently-la beling biological samples. Techniques such as 3D Structured Illumination, Total Internal Reflection Fluorescence and localization microscopy may be used to examine a variety of samples over long periods of time.

    FDA Enforcement
    Class II ·Terminated·GE Healthcare Biosciences·November 28, 2018

    DeltaVision OMX SR Imaging System Model Number: 29115476 The DeltaVision OMX SR Imaging System is a piece of laboratory equipment for super resolution imaging offluorescently-la beling biological samples. Techniques such as 3D Structured Illumination, Total Internal Reflection Fluorescence and localization microscopy may be used to examine a variety of samples over long periods of time.

    FDA Recall
    Terminated ·GE Healthcare Biosciences·Product code REM·September 10, 2018

    ETHILON NYLON SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAR·April 26, 2022

    PIP SZ. 30 PROXIMAL

    FDA Adverse Event
    Malfunction ·ASCENSION ORTHOPEDICS·Product code OMX·October 10, 2017

    PIP SZ. 20 PROXIMAL

    FDA Adverse Event
    Malfunction ·ASCENSION ORTHOPEDICS·Product code OMX·September 14, 2015

    PIP SZ. 20 PROXIMAL

    FDA Adverse Event
    Malfunction ·ASCENSION ORTHOPEDICS·Product code OMX·September 14, 2015

    UNKN PIP IMPL

    FDA Adverse Event
    Injury ·ASCENSION ORTHOPEDICS, INC.·Product code OMX·January 4, 2023

    PIP SZ. 30 PROXIMAL

    FDA Adverse Event
    Malfunction ·ASCENSION ORTHOPEDICS, INC.·Product code OMX·December 4, 2025

    PIP SZ. 20 PROXIMAL

    FDA Adverse Event
    Malfunction ·ASCENSION ORTHOPEDICS·Product code OMX·July 15, 2020

    PIP SZ. 20 PROXIMAL

    FDA Adverse Event
    Malfunction ·ASCENSION ORTHOPEDICS·Product code OMX·July 15, 2020

    PIP SZ. 30 PROXIMAL

    FDA Adverse Event
    Malfunction ·ASCENSION ORTHOPEDICS·Product code OMX·July 15, 2020

    PIP SZ. 30 PROXIMAL

    FDA Adverse Event
    Malfunction ·ASCENSION ORTHOPEDICS·Product code OMX·December 21, 2020

    UNKN MCP IMPL

    FDA Adverse Event
    Injury ·ASCENSION ORTHOPEDICS, INC.·Product code OMX·May 2, 2024

    PIP SZ. 40 PROXIMAL

    FDA Adverse Event
    Malfunction ·ASCENSION ORTHOPEDICS, INC.·Product code OMX·September 22, 2025

    PIP SZ. 20 PROXIMAL

    FDA Adverse Event
    Injury ·ASCENSION ORTHOPEDICS, INC.·Product code OMX·July 18, 2022