412 results
·
32ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
AFX
FDA Adverse Event
Injury
·ENDOLOGIX INC.·Product code MIH·April 19, 2018
AFX
FDA Adverse Event
Injury
·ENDOLOGIX INC.·Product code MIH·April 4, 2018
AFX
FDA Adverse Event
Injury
·ENDOLOGIX·Product code MIH·March 31, 2020
2031527-2012-00113
FDA Adverse Event
Death
·ENDOLOGIX, INC.·December 5, 2012
2031527-2012-00115
FDA Adverse Event
Injury
·ENDOLOGIX, INC.·November 21, 2012
2031527-2012-00119
FDA Adverse Event
Injury
·ENDOLOGIX, INC.·October 30, 2012
2031527-2012-00118
FDA Adverse Event
Injury
·ENDOLOGIX, INC.·December 14, 2012
2031527-2012-00122
FDA Adverse Event
Injury
·ENDOLOGIX, INC.·November 8, 2012
2031527-2012-00120
FDA Adverse Event
Injury
·ENDOLOGIX, INC.·November 21, 2012
2031527-2012-00112
FDA Adverse Event
Injury
·ENDOLOGIX, INC.·December 14, 2012
2031527-2012-00108
FDA Adverse Event
Malfunction
·ENDOLOGIX, INC.·October 29, 2012
2031527-2012-00133
FDA Adverse Event
Death
·ENDOLOGIX, INC.·December 5, 2012
2031527-2012-00094
FDA Adverse Event
Injury
·ENDOLOGIX, INC.·August 15, 2012
2031527-2012-00091
FDA Adverse Event
Injury
·ENDOLOGIX, INC.·August 15, 2012
2031527-2012-00095
FDA Adverse Event
Injury
·ENDOLOGIX, INC.·September 11, 2012
2031527-2012-00109
FDA Adverse Event
Injury
·ENDOLOGIX, INC.·September 26, 2012
2031527-2016-00231
FDA Adverse Event
Injury
·May 19, 2017
AFX
FDA Adverse Event
Injury
·ENDOLOGIX·Product code MIH·July 30, 2018
AFX
FDA Adverse Event
Injury
·ENDOLOGIX·Product code MIH·December 27, 2018
POWERLINK SYSTEM
FDA Adverse Event
Injury
·ENDOLOGIX, INC.·Product code MIH·November 23, 2011