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