5,550 results · 29ms · Sources: EU EUDAMED, US FDA

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TRUE DILATATION CATHETER

FDA Adverse Event
Injury ·BARD PERIPHERAL VASCULAR, INC.·Product code OZT·October 6, 2025

AUDIEN ATOM X HEARING AIDS

FDA Adverse Event
Injury ·AUDIEN /BUDGET HEARING AIDS LLC·Product code QUG·October 23, 2025

AUDIEN ION HEARING AIDS

FDA Adverse Event
Malfunction ·AUDIEN/BUDGET HEARING AIDS, LLC·Product code QUG·August 25, 2025

OLIVE MAX

FDA Adverse Event
Malfunction ·OLIVE UNION INC.·Product code QUG·July 20, 2023

OLIVE MAX

FDA Adverse Event
Malfunction ·OLIVE UNION INC.·Product code QUG·July 20, 2023

NANO CIC DIGITAL RECHARGE HEARING AIDS

FDA Adverse Event
Injury ·NANO HEARING TECH OPCO, LLC·Product code QUG·September 27, 2023

SMART U OTC HEARING AID

FDA Adverse Event
Malfunction ·XIAMEN RETONE HEARING TECHNOLOGY CO., LTD.·Product code QUG·September 5, 2023

HEARING AID

FDA Adverse Event
Malfunction ·MDHEARING WAREHOUSE·Product code QUG·May 6, 2026

NOVA LITE OTC HEARING AID

FDA Adverse Event
Malfunction ·LINNER·Product code QUG·January 18, 2024

JABRA ENHANCE 200 HEARING AID

FDA Adverse Event
Injury ·GN CONSUMER HEARING CORPORATION·Product code QUG·January 17, 2024

PULSE 2 PRO

FDA Adverse Event
Injury ·UNKNOWN·Product code QUG·June 25, 2025

ACOSOUND

FDA Adverse Event
Malfunction ·HANGZHOU ACOSOUND TECHNOLOGY CO.,LTD.·Product code QUG·February 10, 2025

VIVTONE'S XPURE HEARING AIDS

FDA Adverse Event
Injury ·XIAMEN VIENATONE MEDICAL TECHNOLOGY CO., LTD.·Product code QUG·May 13, 2025

AcoSound. Model Number: LW12-BTE-M

FDA Recall
Open, Classified ·HANGZHOU ACOSOUND TECHNOLOGY CO., LTD. No.2 Building Room 401 No.·Product code QUG·April 25, 2025

Hearing Aid, Air-Conduction With Wireless Technology, Over The Counter

FDA classification
FDA Class 2 ·Hearing Aid, Air-Conduction With Wireless Technology, Over The Counter

BUG BITE THING INC.

FDA registration
BUG BITE THING INC.·1 product·🇺🇸 United States

3D Dental

FDA UDI
3D DENTAL DESIGNS AND DEVELOPMENT, LLC·00817169024057·COMPOSITE UNIDOSE DISPENSING GUN

COBAS INTEGRA 400 PLUS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·August 7, 2019

ANKANG OUGELI OPTICAL CO.,LTD

FDA registration
ANKANG OUGELI OPTICAL CO.,LTD·4 products·🇨🇳 China

AUG. HEDINGER GMBH & CO. KG

FDA registration
AUG. HEDINGER GMBH & CO. KG·1 product·🇩🇪 Germany