BEUDAMED
    10 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 ×

    Huvitz Imaging System

    FDA 510(k)
    FDA Class 2 ·Radiology

    ELECTROSURGICAL CUTTING AND COAGULATION DEVICE AND ACCESSORIES

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    THE SONOACE R3 DIAGNOSTIC ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 24, 2025

    Matrixx System

    FDA UDI
    NEXXT SPINE, LLC·00889929065907·Corpectomy, 16Dx18Wx29H 0°

    Matrixx System

    FDA UDI
    NEXXT SPINE, LLC·00889929036952·Corpectomy, 16Dx18Wx29H 6°

    PLUM A+ DRIVER ED 2

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·June 3, 2013

    INFINITI VISION SYSTEM OZIL

    FDA Adverse Event
    Injury ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·July 8, 2011

    CAPSURE SP

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·October 10, 2014

    BEACON TIP TORCON NB ADVANTAGE ANGIOGRAPHIC CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code DQO·November 26, 2025