BEUDAMED
    12 results · 20ms · 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 ×

    LIGHTLAS FAMILY OF MULTI-WAVELENGTH MEDICAL LASER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    CSM INTERNAL-R IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    NEUTRAL LUER ACTIVATED DEVICE AND EXTENSION SETS WITH NEUTRAL LUER ACTIVATED DEVICE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MECTALIF ANTERIOR STAND-ALONE PLATE FLUSH H.12 MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code OVD·March 29, 2018

    AMISTEM H HA COATED STD STEM SIZE 1

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·December 28, 2018

    BUSH URETERAL ILLUMINATING CATHETER SET

    FDA Adverse Event
    Injury ·COOK UROLOGICAL INC·Product code FCS·May 17, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·June 14, 2011

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·August 20, 2008

    STARDRIVE(TM) SCREWDRIVER T15

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HXX·June 13, 2019

    ALIF SCREWDRIVER UNIVERSAL JOINT

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code LXH·January 15, 2016

    MECTALIF ANTERIOR SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code OVD·May 6, 2025

    MECTALIF ANTERIOR TI-PEEK CAGE

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code OVD·January 4, 2018