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 ×

    TRIGEN INTERTAN 10S Nail System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    JMS SYSLOC APHERESIS NEEDLE SET

    FDA UDI
    JMS SINGAPORE PTE LTD·08888483005444·SYSLOC APHERESIS 18GX1" BE 30CM W/CLAMP

    NYOrtho Wheelchair Cushion Gel-Foam 24x18x4

    FDA UDI
    N.Y. ORTHOPEDIC USA, INC.·00811677017853·NYOrtho Gel-Foam Cushions combine a dual chambe...

    POLARIS SPINAL SYSTEM - HA COATED

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    3Delta Crown

    FDA 510(k)
    FDA Class 2 ·Dental

    VISX WAVESCAN WAVEFRONT SYSTEM

    FDA Adverse Event
    Injury ·ADVANCE MEDICAL OPTICS·Product code LZS·November 21, 2008

    ANALYTICAL P MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·September 9, 2011

    DEPUY ASR XL FEM IMP SIZE 46

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KXA·July 22, 2013

    POLARIS SCREW, DIA. 6.5 X UNKNOWN LENGTH

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE, INC.·Product code NKB·May 28, 2025

    POLARIS SCREW, DIA. 6.5 X UNKNOWN LENGTH

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE, INC.·Product code NKB·May 28, 2025

    POLARIS SCREW, DIA. 6.5 X UNKNOWN LENGTH

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE, INC.·Product code NKB·May 28, 2025

    POLARIS SCREW, DIA. 6.5 X UNKNOWN LENGTH

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE, INC.·Product code NKB·May 28, 2025