BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    NeuroBlate System

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ORTHOSTAT BONE HEMOSTAT MATRIX APPLICATOR

    FDA 510(k)
    FDA Unclassified ·Unknown

    DERMA YAG

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    KYPHON INFLATABLE BONE TAMP

    FDA Adverse Event
    Injury ·MEDTRONIC SPINE LLC.·Product code HRX·July 14, 2011

    GYNECARE TVT OBURATOR SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·June 11, 2013

    CONMED

    FDA Adverse Event
    Malfunction ·CONMED ELECTROSURGERY·Product code GEI·September 15, 2008

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code HSD·January 9, 2024

    FOGARTY

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES PR·Product code MJN·March 24, 2025

    EQUINOXE PRESERVE STEM 12MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·May 29, 2019

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·July 2, 2019

    EQUINOXE REVERSE 46MM GLENOSPHERE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·October 2, 2024