BEUDAMED
    13 results · 21ms · 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 ×

    MODIFICATION TO LAPIDUS PLATE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Paltop

    FDA UDI
    PALTOP ADVANCED DENTAL SOLUTIONS LTD·07290108698275·Straight Paltop Equator Abutment Internal Hex. ...

    Orthonol

    FDA UDI
    Rmo, Inc.·00885797016201·ORTHONOL(R) PREFORMED NATURAL ARCH MN .016 X .016

    RADIOTHERAPEUTICS RF 3000 RADIOFREQUENCY GENERATOR

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

    PROTRACT PRESS FIT HIP STEM-HA COATED

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LINEAR 3-4

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 13, 2021

    PERCLOSE¿ PROSTYLE¿

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR INC.·Product code MGB·February 4, 2025

    PERCLOSE PROGLIDE¿

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR INC.·Product code MGB·December 30, 2024

    PERCLOSE¿ PROSTYLE¿

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR INC.·Product code MGB·December 18, 2024

    PERMOBIL C350 CORPUS

    FDA Adverse Event
    Malfunction ·PERMOBIL AB·Product code ITI·April 1, 2013

    ADVIA CENTAUR CP TROPONIN ULTRA ASSAY

    FDA Adverse Event
    SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code MMI·April 27, 2011

    AFFINITY 4

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code HDD·June 30, 2008

    ARMADA 14 PTA CATHETER

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR·Product code DQY·January 2, 2020