BEUDAMED
    1,800 results · 29ms · 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 ×

    UNKNOWN

    FDA Adverse Event
    Injury ·DEPUY SYNTHES SPINE·Product code HWC·January 25, 2018

    UNKNOWN

    FDA Adverse Event
    Injury ·DEPUY SYNTHES SPINE·Product code NKB·January 25, 2018

    CD HORIZON® SOLERA® VOYAGER¿ SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·January 29, 2025

    S4 POLYAXIAL SCREW 6.5X45MM CANULATED

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code NKB·May 7, 2014

    PLIVIOPORE SIZ 10

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code JDN·June 19, 2013

    KYPHX HV-R BONE CEMENT

    FDA Adverse Event
    Injury ·MEDTRONIC SPINE LLC·Product code NDN·June 28, 2010

    3011137372-2017-00105

    FDA Adverse Event
    Injury ·March 16, 2017

    KYPHON XPANDER II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO·Product code HRX·August 31, 2019

    INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, LUMBAR

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code MAX·November 25, 2014

    GUIDE, SURGICAL, INSTRUMENT

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code FZX·August 27, 2015

    UNKNOWN

    FDA Adverse Event
    Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·March 10, 2025

    ACCESS KIT-STERILE

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code KIH·August 23, 2016

    VERTECEM V+ SYRINGE KIT

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code OAR·August 23, 2016

    HYDROLIFT VBR SZ.6 (57-93.5MM)/ENDPL.L

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code MQP·December 3, 2014

    JUVEDERM VOLUMA XC/LIDO (VOLUME UNKNOWN)

    FDA Adverse Event
    Injury ·PRINGY·Product code LMH·December 23, 2024

    SYNCAGE-LR 45º/90º WIDE 12*28*38 PEEK

    FDA Adverse Event
    Malfunction ·SYNTHES BETTLACH·Product code MQP·August 27, 2015

    VERTECEM V+ CEMENT KIT

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code NDN·August 23, 2016

    UNK - ARCOFIX/TELEFIX/VENTROFIX IMPLANTS: TELEFIX

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code MNH·July 15, 2021

    UNK - ARCOFIX/TELEFIX/VENTROFIX IMPLANTS: TELEFIX

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code MNH·July 15, 2021

    UNK - ARCOFIX/TELEFIX/VENTROFIX IMPLANTS: TELEFIX

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code MNH·July 15, 2021