BEUDAMED
    10,000 results · 48ms · 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 ×

    GRAFTON DBM MATRIX STRIPS (DEVICE 1)

    FDA Adverse Event
    Injury ·OSTEOTECH, INC.·Product code MBP·February 17, 2011

    GRAFTON (DBM) MATRIX 2.5CM X 10CM

    FDA Adverse Event
    Injury ·OSTEOTECH·Product code MQV·September 26, 2013

    INFUSE BONE GRAFT DEVICE (RHBMP-2)

    FDA Adverse Event
    Injury ·MEDTRONIC INC·Product code NEK·April 23, 2013

    3.5 LCP SUP CLAV PL LAT EXTN/7H/LT/120

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HRS·August 30, 2021

    CONNEXUS 1CC

    FDA Adverse Event
    Other ·INTEGRA, IRVINE·Product code MQV·May 13, 2011

    ACP KIT SERIES I

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code FMF·November 22, 2019

    UNK - SCREWS: CORTEX

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·August 30, 2021

    UNK - SCREWS: CORTEX

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·August 30, 2021

    UNK - SCREWS: CORTEX

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·August 30, 2021

    UNK - SCREWS: CORTEX

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·August 30, 2021

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·July 1, 2013

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·December 16, 2013

    CD HORIZON® SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO, MED REL·Product code NKB·March 2, 2026

    ANKYLOS C/X IMPLANT B9.5 Ø 4.5/L9.5

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·November 5, 2015

    ANKYLOS C/X IMPLANT A 9.5 Ø 3.5 /L 9.5

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·November 5, 2015

    ANKYLOS C/X IMPLANT A 9.5 Ø 3.5 /L 9.5

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·November 5, 2015

    ANKYLOS C/X IMPLANT B9.5 Ø 4.5/L9.5

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·November 5, 2015

    ANKYLOS C/X IMPLANT A 9.5 Ø 3.5 /L 9.5

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·November 5, 2015

    ANKYLOS C/X IMPLANT A 9.5 Ø 3.5 /L 9.5

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·November 5, 2015

    ANKYLOS C/X IMPLANT A 9.5 Ø 3.5 /L 9.5

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·November 5, 2015