13 results
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18ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Injury
×
INPLANT FUNNEL
FDA Adverse Event
Injury
·PROXIMATE CONCEPTS LLC·Product code KDD·May 7, 2021
INPLANT FUNNEL
FDA Adverse Event
Injury
·PROXIMATE CONCEPTS LLC·Product code KDD·May 10, 2021
INPLANT FUNNEL
FDA Adverse Event
Injury
·PROXIMATE CONCEPTS LLC·Product code KDD·May 10, 2021
INPLANT FUNNEL
FDA Adverse Event
Injury
·PROXIMATE CONCEPTS LLC·Product code KDD·May 7, 2021
INPLANT FUNNEL
FDA Adverse Event
Injury
·PROXIMATE CONCEPTS LLC·Product code KDD·May 10, 2021
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS LLC (PR)·Product code NIQ·April 5, 2011
6F ANGIO-SEAL VASCULAR CLOSURE DEVICE VIP
FDA Adverse Event
Injury
·ST. JUDE MEDICAL·Product code MGB·May 7, 2008
OPTETRAK LOGIC KNEE COMPONENTS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·June 23, 2025
LOGIC CR TIB INSERT STD, SZ 2, 9MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·January 17, 2025
LOGIC TIB INSERT IMPL CRC, SZ 2, 9MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·June 28, 2023
THREE PEG PATELLA 32MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·January 28, 2026
SPECIFIC DEVICE NOT REPORTED
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·December 13, 2024
OPTETRAK LOGIC
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·April 16, 2025