BEUDAMED
    12 results · 22ms · 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 ×

    DP4 Microneedling device

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

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111318702·METZENBAUM SCISS DEL CVD 7"

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197474443·Beckmann adenoid curette Fig. 7...

    C-QUR RPM MESH

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

    KMTI S141 Lumbar Interbody Fusion System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BONE SCREWS

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code MBF·February 25, 2026

    UNIFY CRT-D, DF-4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NIK·November 3, 2014

    GORE PRECLUDE DURA SUBSTITUTE

    FDA Adverse Event
    Injury ·W. L. GORE ASSOCIATES INC.·Product code GXQ·July 2, 2013

    BATTERY 14.8V, 6.3 AH LI-ION BATTERY

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·November 12, 2015

    RED DISTAL FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·March 20, 2018

    WOUND DRAINAGE

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code GCY·December 12, 2024

    CHANNEL DRAIN

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code GBX·December 11, 2024