BEUDAMED
    105 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.

    FOUNDERS OPTICAL GROUP, LLC

    FDA registration
    FOUNDERS OPTICAL GROUP, LLC·1 product·🇺🇸 United States

    Eko CORE 500 Founder's Edition Chestpiece

    FDA UDI
    Eko Devices, Inc.·00850010298214·Eko CORE 500 Founder's Edition Chestpiece

    REAMER HANDLE OFFSET

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL CORP.·Product code OLO·December 8, 2025

    Eko CORE 500 and CAC500 Founder's Edition bundle

    FDA UDI
    Eko Devices, Inc.·00850010298207·

    FORTIUS 420 HYPERBARIC CHAMBER

    FDA Adverse Event
    Death ·OXYHEALTH, LLC.·Product code CBF·July 15, 2025

    BARD® DIGNISHIELD® STOOL MANAGEMENT SYSTEM

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KNT·May 17, 2024

    BARD® DIGNISHIELD® STOOL MANAGEMENT SYSTEM

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KNT·May 24, 2024

    BARD® DIGNISHIELD® STOOL MANAGEMENT SYSTEM

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KNT·May 24, 2024

    BARD® DIGNISHIELD® STOOL MANAGEMENT SYSTEM

    FDA Adverse Event
    Malfunction ·C.R. BARD INC. (COVINGTON) -1018233·Product code KNT·May 16, 2024

    SUROS SURGICAL

    FDA Adverse Event
    Other ·SUROS SURGICAL·Product code KNW·March 15, 2005

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·March 21, 2011

    SPINE-TECH BAK INTERBODY FUSION DEVICE

    FDA Adverse Event
    Other ·SULZER SPINE-TECH·Product code MAX·November 3, 1999

    23 AND ME HEALTH EDITION

    FDA Adverse Event
    Other ·23 AND ME, INC.·Product code MAO·December 3, 2009

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 6, 2011

    ASHLEY BLACK FASCIABLASTER

    FDA Adverse Event
    Injury ·ADB INTERESTS, LLC·Product code IOD·April 29, 2017

    BARD® DIGNISHIELD® STOOL MANAGEMENT SYSTEM

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code KNT·May 23, 2024

    VERSACARE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·August 3, 2015

    VERSACARE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·June 15, 2015

    VERSACARE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·June 15, 2015

    TSI - OCO BIOMEDICAL INC. DENTAL IMPLANT

    FDA Adverse Event
    Other ·OCO BIOMEDICAL, INC.·Product code DZE·May 5, 2008