2,113 results
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35ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Humeral Plating System
FDA UDI
SKELETAL DYNAMICS L.L.C.·00841506110004·
CURLIN INFUSION ADMINISTRATION SET
FDA Adverse Event
Malfunction
·,OOG·Product code FRN·November 12, 2014
CAS PSI KNEE SYSTEM
FDA Adverse Event
Injury
·ZIMMER CAS·Product code JWH·August 18, 2016
PSI KNEE SYSTEM
FDA Adverse Event
Injury
·ZIMMER CAS·Product code JWH·August 18, 2016
UNK KNEE STEM ATTUNE REVISION
FDA Adverse Event
Injury
·DEPUY IRELAND - 9616671·Product code JWH·February 13, 2024
CAS PSI KNEE SYSTEM
FDA Adverse Event
Injury
·ZIMMER CAS·Product code JWH·August 18, 2016
CAS PSI KNEE SYSTEM
FDA Adverse Event
Injury
·ZIMMER CAS·Product code OOG·August 18, 2016
CAS PSI KNEE SYSTEM
FDA Adverse Event
Injury
·ZIMMER CAS·Product code JWH·August 18, 2016
UNK ATTUNE KNEE PATELLA
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JWH·February 13, 2024
UNK KNEE STEM ATTUNE REVISION
FDA Adverse Event
Injury
·DEPUY IRELAND - 9616671·Product code JWH·February 13, 2024
UNKNOWN KNEE FEMORAL AUGMENT
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JWH·February 13, 2024
UNKNOWN KNEE FEMORAL AUGMENT
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JWH·February 13, 2024
UNK KNEE TIBIAL TRAY ATTUNE REVISION
FDA Adverse Event
Injury
·DEPUY IRELAND - 9616671·Product code JWH·February 13, 2024
UNK KNEE TIBIAL INSERT ATTUNE REVISION
FDA Adverse Event
Injury
·DEPUY IRELAND - 9616671·Product code JWH·February 13, 2024
UNK KNEE FEMORAL ATTUNE REVISION
FDA Adverse Event
Injury
·DEPUY IRELAND - 9616671·Product code JWH·February 13, 2024
ITOTAL
FDA Adverse Event
Injury
·CONFORMIS·Product code OOG·July 31, 2015
OTISKNEE CUTTING GUIDE - STRYKER
FDA Adverse Event
Malfunction
·OTISMED CORP·Product code OOG·February 19, 2010
OTISKNEE CUTTING GUIDE - STRYKER
FDA Adverse Event
Malfunction
·OTISMED CORP·Product code OOG·February 19, 2010
OTISKNEE CUTTING GUIDE - BIOMET - RIGHT
FDA Adverse Event
Malfunction
·OTISMED CORP·Product code OOG·February 19, 2010
OTISKNEE CUTTING GUIDE - STRYKER
FDA Adverse Event
Malfunction
·OTISMED CORPORATION·Product code OOG·February 19, 2010