BEUDAMED
    26 results · 23ms · 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 ×

    LAA Exclusion System

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

    Alteon

    FDA UDI
    Exactech, Inc.·10885862517715·ALTEON MONO REVSTM TRIAL SIZE 23X295

    GENESIS II POSTERIOR STABILIZED HIGH FLEXION ARTICULAR INSERT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    21HQ513D

    FDA 510(k)
    FDA Class 2 ·Radiology

    KANGAROO

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, LLC·Product code KNT·December 11, 2025

    KANGAROO

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, LLC·Product code KNT·July 29, 2025

    KANGAROO

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH, INC.·Product code KNT·June 5, 2025

    KANGAROO

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, LLC·Product code KNT·June 5, 2025

    KANGAROO

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, LLC·Product code KNT·July 29, 2025

    KANGAROO

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, LLC·Product code KNT·December 11, 2025

    KANGAROO

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, LLC·Product code KNT·May 12, 2025

    KANGAROO

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, LLC·Product code KNT·January 26, 2026

    PERIMOUNT MAGNA EASE AORTIC SIZER

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES·Product code DTI·November 5, 2008

    MEDTRONIC

    FDA Adverse Event
    Injury ·MEDTRONIC INC·Product code DTB·August 26, 2011

    RESTYLANE, RESTYLANE

    FDA Adverse Event
    Injury ·Q-MED·Product code LMH·July 11, 2013

    KANGAROO

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, LLC·Product code KNT·May 7, 2025

    KANGAROO

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH, INC.·Product code KNT·June 12, 2025

    KANGAROO

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH, INC.·Product code KNT·June 12, 2025

    GII ARTICULAR INSERTER/EXTRACT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBH·February 9, 2018

    KANGAROO

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH, INC.·Product code KNT·June 12, 2025