BEUDAMED
    13 results · 31ms · 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 ×

    LOSPA IS Spinal System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517575418·CoRoent Ant TLIF Ti, 15x11x40mm 8°

    ProLift Trial

    FDA UDI
    Life Spine, Inc.·00190837087500·

    MICROGARD II

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    INTELIFUSE, INC. WARM SYSTEM WITH STIMULINKS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VERSYS FEMORAL STEM

    FDA Adverse Event
    Injury ·ZIMMER INC·Product code LPH·February 25, 2016

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 12, 2025

    GMK PRIMARY FEMUR CEMENTED PS #5NARROW / LEFT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·November 25, 2015

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 30, 2013

    MAYFIELD TRIAD SKULL CLAMP

    FDA Adverse Event
    Malfunction ·INTEGRA, CINCINNATI·Product code HBL·June 21, 2011

    HIRES 90K

    FDA Adverse Event
    Injury ·ADVANCED BIONICS LLC·Product code MCM·September 4, 2008

    GMK-SPHERE FEMORAL COMPONENT CEMENTED SIZE 4 RIGHT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·September 7, 2016

    Medical Linear Accelerator

    FDA Enforcement
    Class II ·Terminated·Elekta, Inc.·September 14, 2016