BEUDAMED
    41 results · 22ms · Sources: EU EUDAMED, US FDA

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    Flow-Nail

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TALOS° HA PEEK IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1676221115150·

    TALOS° HA PEEK IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1676221115070·

    TALOS° HA PEEK IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1676221115000·

    Luna

    FDA UDI
    ULTRADENT PRODUCTS, INC.·00883205004017·Luna Opal MB Mini .022 LL3 D/HK (-6°T +3°A)

    PEDICLE SCREW 7X45

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·April 10, 2018

    PEDICLE SCREW 7X50

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·February 23, 2018

    PEDICLE SCREW 5X45

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·March 23, 2018

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523134113·Tesera ST, 22mm X 11mm X 15mm, Convex, T3

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523149285·Straight Implant Trial 22mm x 11mm x 15mm

    GYNEFLEX

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    M.U.S.T PEDICLE SCREW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    M.U.S.T. RODS

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·April 20, 2026

    PEDICLE SCREW PEDICLE SCREW 5X40

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·January 17, 2024

    M.U.S.T. POLYAXIAL PEDICLE SCREW

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MNI·October 28, 2024

    MUST PEDICLE SCREW 8X40MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·November 22, 2017

    PEDICLE SCREW - PEDICLE SCREW 8X75MM

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code NKB·October 11, 2018

    PEDICLE SCREW PEDICLE SCREW 7X45

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·September 9, 2022

    MECTALIF OBLIQUE (TI PEEK) INTERBODY FUSION DEVICE 12X28X11 L10

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MAX·April 1, 2020

    M.U.S.T. PEDICLE SCREW 7X45

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MNI·January 20, 2017