BEUDAMED
    9 results · 24ms · Sources: EU EUDAMED, US FDA

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    BIASURGE Advanced Surgical Solution

    FDA 510(k)
    FDA Unclassified ·Unknown

    TARGET DETACHABLE COIL

    FDA 510(k)
    FDA Class 2 ·Neurology

    ORIA CERVICAL PLATES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    INCLUSIVE MINI IMPLANT O-BALL 2.2 MMD X 10 MML

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·April 21, 2025

    UNK ZIMMER TM REVERSE SHOULDER

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code HSD·October 29, 2014

    LONG ROUND DIAMOND BUR

    FDA Adverse Event
    Malfunction ·CONMED LINVATEC·Product code HWE·August 25, 2011

    OT VERIO PRO PLUS METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 12, 2013

    MAKO Integrated Cutting System (MICS) HANDPIECE, Catalog Number 209063

    FDA Enforcement
    Class II ·Ongoing·Howmedica Osteonics Corp.·October 16, 2024

    SpF PLUS-Mini (60 ¿A/W) Implantable Spinal Fusion Stimulator SpF PLUS-Mini Implantable Fusion Stimulators are indicated as a spinal fusion adjunct to increase the probability of fusion success in 1 or 2 levels

    FDA Enforcement
    Class I ·Terminated·Zimmer Biomet, Inc.·November 7, 2018