10,000 results
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151ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CAUSSE LARGE LOOP PISTON
FDA Adverse Event
Other
·MEDTRONIC XOMED, INC.·Product code FZD·December 5, 2008
CAUSSE LARGE LOOP PISTON
FDA Adverse Event
Other
·MEDTRONIC XOMED, INC.·Product code FZD·December 5, 2008
MEDPOR EXTERNAL EAR IMPLANT
FDA Adverse Event
Malfunction
·POREX SURGICAL, INC.·Product code FZD·June 11, 1997
PROSTHESIS
FDA Adverse Event
Injury
·MEDTRONIC XOMED INC.·Product code FZD·December 29, 2020
OMNIPORE SURGICAL IMPLANT
FDA Adverse Event
Injury
·MATRIX SURGICAL USA·Product code FZD·December 7, 2021
OMNIPORE SURGICAL IMPLANT
FDA Adverse Event
Injury
·MATRIX SURGICAL USA·Product code FZD·September 1, 2021
OMNIPORE SURGICAL IMPLANT
FDA Adverse Event
Injury
·MATRIX SURGICAL USA·Product code FZD·September 1, 2021
OMNIPORE SURGICAL IMPLANT
FDA Adverse Event
Injury
·MATRIX SURGICAL USA·Product code FZD·February 1, 2023
SOUNDTEC IMPLANT
FDA Adverse Event
Injury
·SOUNDTEC INC·Product code FZD·January 3, 2005
SOUND TEC IMPLANT
FDA Adverse Event
Injury
·SOUND TEC INC.·Product code FZD·January 3, 2005
HYDROXYLAPATITE AND FLEX H/A/
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED·Product code FZD·November 17, 2015
Prosthesis, Ear, Internal
FDA classification
FDA Class 2
·Prosthesis, Ear, Internal
BROAD NEEDLE ELECTRODE
FDA UDI
Cynosure, LLC·00841494102289·BROAD NEEDLE ELECTRODE - 25PCS STERILE
DIVERSITY CORPORATION FZE
FDA registration
DIVERSITY CORPORATION FZE·20 products·🇦🇪 United Arab Emirates
SURGYMED TRADING FZE
FDA registration
SURGYMED TRADING FZE·3 products·🇦🇪 United Arab Emirates
FMD. Co., Ltd.
FDA registration
FMD. Co., Ltd.·1 product·🇯🇵 Japan
DUROSCOPE
FDA UDI
FMD, LLC·00863333000310·LED Light source
DUROSCOPE
FDA UDI
FMD, LLC·00863333000334·UHD Camera
DUROSCOPE
FDA UDI
FMD, LLC·00863333000341·Fiber Optic Light Guide
DUROSCOPE
FDA UDI
FMD, LLC·00863333000327·FHD Camera