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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    BURR, CORNEAL, BATTERY-POWERED

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    OsteoCentric Navigated Instruments System

    FDA 510(k)
    FDA Class 2 ·Neurology

    DARCO Locking Bone Plate System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BIOMET TIBIAL LOCKING BAR

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·February 22, 2018

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·February 8, 2013

    ACUITY

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code OJX·January 6, 2011

    HEARTMATE II LVAS

    FDA Adverse Event
    Injury ·THORATEC CORP.·Product code DSQ·July 11, 2014