13 results
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36ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Injury
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PTERYFIT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·December 19, 2024
PTERYFIT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·December 18, 2024
PTERYFIT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·January 16, 2025
PTERYFIT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·November 17, 2024
PTERYFIT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·April 16, 2025
PTERYFIT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·November 17, 2024
PTERYFIT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·April 16, 2025
PTERYFIT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·August 10, 2025
M2A MAGNUM MODULAR HEAD 42MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·November 22, 2011
M2A MAGNUM PF CUP 48MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDIC·Product code KWA·November 22, 2011
TAPERLOC POROUS LATERALIZED FEMORAL 9X137
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LPH·November 22, 2011
M2A MAGNUM TAPER ADAPTER
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·November 22, 2011
EEA 31MM SINGLE-USE STAPLER
FDA Adverse Event
Injury
·NORTH HAVEN-USS·Product code GAG·February 20, 2008