BEUDAMED
    55 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 ×

    CLEARFIL MAJESTY FLOW

    FDA 510(k)
    FDA Class 2 ·Dental

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHE USA·Product code HWC·April 9, 2015

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·September 23, 2015

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·September 23, 2015

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·October 7, 2015

    FLAATZ 560

    FDA 510(k)
    FDA Class 2 ·Radiology

    PATXFER

    FDA 510(k)
    FDA Class 2 ·Radiology

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·June 16, 2016

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·November 13, 2014

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES SELZACH·Product code HWC·June 2, 2015

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·January 5, 2016

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·July 30, 2015

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·February 15, 2017

    ORION RC SCS IPG

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code LGW·November 3, 2023

    SCREW LOCKING

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HWC·March 14, 2012

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HWC·March 14, 2012

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES OBERDORF·Product code HWC·March 14, 2012

    ATTAIN OTW

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·June 13, 2011

    GYNECARE MORCELLEX* TISSUE MORCELLATOR

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code HET·May 21, 2013

    ECHELON 60 ENDOPATH STAPLER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GDW·August 8, 2008