30 results · 23ms · Sources: EU EUDAMED, US FDA

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NeuroStar, NeuroStar TMS Therapy System, NeuroStar Advanced Therapy System, NeuroStar Advanced Therapy System for Mental Health

FDA 510(k)
FDA Class 2 ·Neurology

NORMED MINI EXTERNAL FIXATOR SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

NEXXT MATRIXX Stand Alone ALIF System

FDA 510(k)
FDA Class 2 ·Orthopedic

ADVIA 2120

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code GKL·August 24, 2011

SYNCHROMED II

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·November 3, 2014

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·July 12, 2013

INFUSE BONE GRAFT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·March 1, 2012

INFUSE BONE GRAFT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·March 1, 2012

INFUSE BONE GRAFT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·March 1, 2012

INFUSE BONE GRAFT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·March 1, 2012

INFUSE BONE GRAFT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·March 1, 2012

INFUSE BONE GRAFT

FDA Adverse Event
Death ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·March 1, 2012

INFUSE BONE GRAFT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·March 1, 2012

INFUSE BONE GRAFT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·March 1, 2012

INFUSE BONE GRAFT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·March 1, 2012

SELECTSECURE MRI SURESCAN

FDA Adverse Event
Malfunction ·MEDTRONIC, INC.·Product code NVN·September 9, 2022

MEDTRONIC LEAD

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code DXY·September 9, 2022

TM REVERSE 36MM GLENOSPHERE

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code PHX·September 19, 2025

TM RVS BASE PLT 25MM POST +2

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code PHX·September 19, 2025

CLOSUREFAST CATHETER

FDA Adverse Event
Injury ·COVIDIEN·Product code GEI·September 22, 2021