BEUDAMED
    15 results · 21ms · 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 ×

    SYNEA-HS HIGH SPEED-HANDPIECE

    FDA 510(k)
    FDA Class 1 ·Dental

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756609777·PHILADELPHIA COLLAR

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694090872·2.0 x 11mm IMF AutoDrive Screw

    SCOTT'S SELECT MICROHYBRID SYRINGE 4.5 Gm (A4)

    FDA UDI
    SCOTT'S DENTAL SUPPLY L.L.C.·D77819920110·Scott’s Select Microhybrid Composite is indicat...

    NORM SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PhoeniX

    FDA 510(k)
    FDA Class 2 ·Radiology

    RADIFOCUS OPTITORQUE

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·June 13, 2022

    SCREW,FIXATION,BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·May 18, 2015

    OXF UNI TIB TRAY SZ D RM PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·May 30, 2019

    OXF ANAT BRG RT LG SIZE 3 PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·May 30, 2019

    1.5MM MANDIBLE MESH FOOT B-TYPE FOR CMF DISTRACTOR

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code MQN·March 7, 2013

    REVEAL DX

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DSI·February 15, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 8, 2014

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·July 27, 2015

    OPTITORQUE ANGIOGRAPHIC CATHETER

    FDA Adverse Event
    Malfunction ·Product code DQO·January 20, 2021