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