BEUDAMED
    8 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 ×

    PROSTEP MICA Screw System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NUVASIVE SURGICAL MESH SYSTEM

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

    SMITH & NEWPHEW ULTRABRAID II SUTURE

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

    INVICTUS SPINAL FIXATION SYSTEM

    FDA Adverse Event
    Injury ·ALPHATEC SPINE, INC.·Product code NKB·April 30, 2025

    PADGETT MODEL S SLIMLINE ELECTRIC DERMATOME

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES CORPORATION OH/USA·Product code GFD·June 14, 2013

    NOVOTTF-100A

    FDA Adverse Event
    Injury ·NOVOCURE LTD·Product code NZK·September 24, 2014

    TALENT CAPTIVIA FF

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR IRELAND·Product code MIH·July 21, 2011

    PENUMA IMPLANT

    FDA Adverse Event
    Injury ·INTERNATIONAL MEDICAL DEVICES, INC.·Product code MIB·October 7, 2019