10,000 results · 63ms · Sources: EU EUDAMED, US FDA

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I Do

FDA 510(k)
FDA Class 2 ·Dental

EBM IDO VIEWER

FDA 510(k)
FDA Class 2 ·Radiology

EBM iDO Viewer 1.2.1

FDA 510(k)
FDA Class 2 ·Radiology

EBM

FDA UDI
EBM TECHNOLOGIES INCORPORATED·04719878870191·

EBM

FDA UDI
EBM TECHNOLOGIES INCORPORATED·04719878870290·

I DO NOT KNOW

FDA Adverse Event
Injury ·Product code FTL·August 22, 2010

FIXODENT

FDA Adverse Event
Injury ·Product code KOL·June 23, 2009

PWRD ECH FLEX 45MM 34CM SHAFT

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·October 22, 2020

ULTRASONIC SCALER I DO NOT KNOW THE BRAND NAME

FDA Adverse Event
Other ·*·Product code ELC·June 8, 2005

CO2 LASER ( I DO NOT KNOW THE BRAND NAME)

FDA Adverse Event
Injury ·ROHRER AESTHETICS, INC.·Product code GEX·July 16, 2025

XIA 3 TITANIUM BLOCKER

FDA Adverse Event
Malfunction ·STRYKER SPINE-SWITZERLAND·Product code MNH·September 6, 2016

XIA 3 TITANIUM BLOCKER

FDA Adverse Event
Malfunction ·STRYKER SPINE-SWITZERLAND·Product code MNH·September 6, 2016

ESSURE

FDA Adverse Event
Injury ·BAYER·Product code HHS·June 16, 2014

GUIDANT

FDA Adverse Event
Injury ·GUIDANT·Product code LWS·July 21, 2005

PROLENE SUTURE 36"(90CM) 5-0 BLU

FDA Adverse Event
Malfunction ·ETHICON INC.·Product code GAW·June 1, 2021

PROLENE SUTURE 36"(90CM) 5-0 BLU

FDA Adverse Event
Malfunction ·ETHICON INC.·Product code GAW·June 1, 2021

BD NEXIVA¿ CLOSED IV CATHETER

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·March 9, 2023

FREESTYLE LIBRE 3 PLUS

FDA Adverse Event
Malfunction ·ABBOTT DIABETES CARE INC.·Product code QBJ·December 16, 2025

FREESTYLE LIBRE 3 PLUS

FDA Adverse Event
Malfunction ·ABBOTT DIABETES CARE INC.·Product code QBJ·December 16, 2025

EVERA MRI XT DR

FDA Adverse Event
Death ·MEDTRONIC, INC.·Product code LWS·October 16, 2023