BEUDAMED
    13 results · 27ms · 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 ×

    Overwatch Spine System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NYOrtho APEX CORE Wedge Pommel Wheelchair Cushion Foam 16x18x4x2

    FDA UDI
    N.Y. ORTHOPEDIC USA, INC.·00810114601969·For patients requiring hip positioning that are...

    Drill Stopper for Long L16 1842

    FDA UDI
    ADIN DENTAL IMPLANT SYSTEMS LTD·07290105157454·

    QUANTA LITE PBC SCREEN IGG/IGA ELISA

    FDA 510(k)
    FDA Class 2 ·Immunology

    ACIES

    FDA 510(k)
    FDA Class 2 ·Radiology

    Matrixx System

    FDA UDI
    NEXXT SPINE, LLC·00889929066034·Corpectomy, 16Dx18Wx42H 0°

    Matrixx System

    FDA UDI
    NEXXT SPINE, LLC·00889929037027·Corpectomy, 16Dx18Wx42H 6°

    CONCERTO II CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·October 10, 2014

    INTEGRIS V3000

    FDA Adverse Event
    Injury ·PHILIPS HEALTHCARE·Product code IZI·July 8, 2011

    PFNA BLADE L130 TAN

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code JDS·June 11, 2013

    BEACON TIP TORCON NB ADVANTAGE ANGIOGRAPHIC CATHETER

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

    GMK-HINGE FIXED TIBIAL INSERT SIZE 4/12MM

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code KRO·February 23, 2017

    GMK-HINGE FIXED TIBIAL INSERT SIZE 4/12MM

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code KRO·April 6, 2017