6 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
HEARTMATE II SYSTEM CONTROLLER
FDA Adverse Event
Malfunction
·THORATEC CORP·Product code DSQ·April 11, 2014
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·November 2, 2012
HARMONIC ACE 36 CM
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC (CINCINNATI)·Product code LFL·August 17, 2007
MECTALIF OBLIQUE (TI PEEK)OBLIQUE INTERBODY FUSION DEVICE PEEK/TI 12X28X13 L10°
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code MAX·February 5, 2024
OPTETRAK LOGIC KNEE COMPONENTS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·February 12, 2025
THREE PEG PATELLA 32MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·July 3, 2024