BEUDAMED
    7 results · 20ms · 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 ×

    Sempulse Halo Vital Signs Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    THE LIFECORE STAGE-1 ANGLED ABUTMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    SIRION Lateral Lumbar Interbody Fusion

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DEXCOM G6 GLUCOSE PROGRAM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 21, 2025

    GE OEC 9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·November 13, 2008

    COMPREHENSIVE SHOULDER INSTRUMENTS PRIMARY SHOULDER STEM INSERTER

    FDA Adverse Event
    BIOMET ORTHOPEDICS·Product code LXH·September 2, 2011

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·July 18, 2013