824 results · 41ms · Sources: EU EUDAMED, US FDA

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CLARION II HI-RES COCHLEAR IMPLANT

FDA Adverse Event
Injury ·ADVANCED BIONICS·Product code MCM·July 30, 2005

HI (BTE)

Basic UDI-DI
EU MDR · Eu Md Class 2a ·SBO Hearing A/S·221 devices

HI (BTE)

Basic UDI-DI
EU MDR · Eu Md Class 2a ·SBO Hearing A/S·126 devices

HI (BTE)

Basic UDI-DI
EU MDR · Eu Md Class 2a ·SBO Hearing A/S·2050 devices

HI (BTE)

Basic UDI-DI
EU MDR · Eu Md Class 2a ·SBO Hearing A/S·1253 devices

HI (BTE)

Basic UDI-DI
EU MDR · Eu Md Class 2a ·SBO Hearing A/S·1525 devices

HI (BTE)

Basic UDI-DI
EU MDR · Eu Md Class 2a ·SBO Hearing A/S·610 devices

MED-EL COMBI 40+ CPCHLEAR IMPLANT SYSTEM

FDA Adverse Event
Malfunction ·MED-EL ELEKTROMEDIZINISCHE GERAETE, GMBH·Product code MCM·December 2, 2009

SONIC INNOVATIONS, INC.

FDA Adverse Event
Malfunction ·SONIC INNOVATIONS, INC.·Product code ESD·March 19, 2012

ACTIVA

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·March 17, 2017

RESOUND

FDA Adverse Event
Injury ·GN HEARING A/S·Product code OSM·April 27, 2022

RESOUND

FDA Adverse Event
Injury ·GN HEARING A/S·Product code OSM·April 1, 2022

GN RESOUND

FDA Adverse Event
Injury ·GN HEARING A/S·Product code OSM·July 14, 2022

HILT FAMILY LASER: HILT I, HILT II, HILT III

FDA 510(k)
FDA Class 2 ·Physical Medicine

IBT Scientific

FDA registration
IBT Scientific·5 products·🇺🇸 United States

HINT AUDIOMETER, OR HINT

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

Power Dental USA

FDA UDI
Power Dental U.S.A. Inc.·D9439008BIBT00·PERIOSTEAL ELEVATORS SET (11 PCS)

Dream by 3D Dental

FDA UDI
3D DENTAL DESIGNS AND DEVELOPMENT, LLC·00817169028000·DREAM INTERDENTAL BRUSH TAPERED BOX/72 GREEN

HIP Cleaning Solution

FDA UDI
Dent4You AG·07640397422332·Hydrim Cleaning Solution with Instrument Protec...

'HILT-WAY' RESUSCITATOR

FDA 510(k)
FDA Class 1 ·Anesthesiology