BEUDAMED
    155 results · 64ms · 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.

    KOREA BODY INFORMATION

    FDA registration
    KOREA BODY INFORMATION·1 product·🇰🇷 South Korea

    I-PORT ADVANCE

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·August 28, 2025

    MITEK EXPRESSEW

    FDA Adverse Event
    Malfunction ·DEPUY MITEK·Product code LXH·November 18, 2013

    SILHOUETTE PARADIGM

    FDA Adverse Event
    Malfunction ·Product code FPA·November 7, 2022

    COUGAR LS 18X8X50 LORDOTIC

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL CH·Product code MAX·June 21, 2022

    PROSTHESIS, INTERVERTEBRAL DISC

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code MJO·May 19, 2015

    THUNDERBEAT 5 MM, 20 CM, FRONT-ACTUATED GRIP TYPE S

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code GEI·September 6, 2023

    UNKNOWN SCREW/ROD CONSTRUCT ACCESSORIES

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SàRL CH·Product code MNH·June 30, 2021

    UNKNOWN SCREW/ROD CONSTRUCT ACCESSORIES

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SàRL CH·Product code MNH·July 1, 2021

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HWC·August 6, 2019

    MESH, SURGICAL

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code FTM·August 6, 2019

    MESH, SURGICAL

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code FTM·August 6, 2019

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HRS·May 2, 2017

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·March 26, 2026

    THUNDERBEAT 5 MM, 35 CM, FRONT-ACTUATED GRIP TYPE S

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code GEI·September 14, 2023

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·May 1, 2017

    SHAFT COMPL.D:10MM L:370MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code OCW·September 23, 2016

    DYNA LOCKING TROCHANTERIC NAIL

    FDA Adverse Event
    Injury ·U&I CORPORATION·Product code HSB·December 3, 2019

    MOTIVA IMPLANTS

    FDA Adverse Event
    Injury ·ESTABLISHMENT LABS S.A.·Product code FTR·April 28, 2025

    MOTIVA IMPLANTS

    FDA Adverse Event
    Injury ·ESTABLISHMENT LABS S.A.·Product code FTR·May 7, 2025