24 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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INVISION Total Ankle Revision System
FDA 510(k)
FDA Class 2
·Orthopedic
INVISION¿ TOTAL ANKLE SYSTEM
FDA Adverse Event
Injury
·WRIGHT MEDICAL TECHNOLOGY INC·Product code HSN·July 18, 2022
BACTRACK LCD ALCOHOL DETECTOR
FDA 510(k)
FDA Class 1
·Clinical Toxicology
SURESIGNS VM4, SURESIGNS VM6, SURESIGNS VM8 MODEL: 863063, 863064, 863065, 863066, 863068
FDA 510(k)
FDA Class 2
·Cardiovascular
BIZACT
FDA Adverse Event
Injury
·COVIDIEN MFG DC BOULDER·Product code GEI·June 18, 2019
EQUINOXE
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWT·February 6, 2019
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·INVACARE REHABILITATION EQUIP·Product code FSA·October 14, 2014
STARCLOSE VASCULAR CLOSURE SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·June 14, 2013
SAGITTAL BLADE
FDA Adverse Event
Malfunction
·STRYKER IRELAND LTD.·Product code GFA·June 29, 2011
BIZACT
FDA Adverse Event
Malfunction
·COVIDIEN MFG DC BOULDER·Product code GEI·April 30, 2024
BIZACT
FDA Adverse Event
Malfunction
·COVIDIEN MFG DC BOULDER·Product code GEI·April 30, 2024
BIZACT
FDA Adverse Event
Injury
·COVIDIEN MFG DC BOULDER·Product code GEI·October 19, 2020
BIZACT
FDA Adverse Event
Injury
·COVIDIEN MFG DC BOULDER·Product code GEI·October 19, 2020
BIZACT
FDA Adverse Event
Injury
·COVIDIEN MFG DC BOULDER·Product code GEI·October 19, 2020
BIZACT
FDA Adverse Event
Injury
·COVIDIEN MFG DC BOULDER·Product code GEI·October 21, 2020
BIZACT
FDA Adverse Event
Malfunction
·COVIDIEN MFG DC BOULDER·Product code GEI·April 30, 2024
BIZACT
FDA Adverse Event
Malfunction
·COVIDIEN MFG DC BOULDER·Product code GEI·May 2, 2024
BIZACT
FDA Adverse Event
Malfunction
·COVIDIEN MFG DC BOULDER·Product code GEI·May 24, 2024
BIZACT
FDA Adverse Event
Malfunction
·COVIDIEN MFG DC BOULDER·Product code GEI·April 25, 2024
BIZACT
FDA Adverse Event
Malfunction
·COVIDIEN MFG DC BOULDER·Product code GEI·May 17, 2024