17 results
·
35ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
WAVEWRITER ALPHA
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·May 28, 2024
QUILL SRS
FDA Adverse Event
Other
·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·April 30, 2009
QUILL SRS
FDA Adverse Event
Other
·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·April 30, 2009
QUILL SRS
FDA Adverse Event
Other
·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·August 24, 2009
UNKNOWN DEPUY FEMORAL COMPONENT
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC./REG. #1818910·Product code JWH·April 26, 2013
EON RECHARGEABLE IPG, 16-CHANNEL
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·April 25, 2011
SOFTCLIX LANCET DEVICE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code FMK·July 22, 2008
QUILL SRS
FDA Adverse Event
Other
·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·March 12, 2009
OSS 9CM PROX TIB MOD COCR
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KRO·July 2, 2025
OSS TIBIAL POLY BEARING 12MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·July 2, 2025
OSS POLY LOCK PIN
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·July 2, 2025
OSS POLY FEMORAL BUSHINGS
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·July 2, 2025
OSS REINFORCED YOKE
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KRO·July 2, 2025
OSS POLY TIBIAL BUSHING
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·July 2, 2025
OSS CMNTD PROX TIB STEM 11X150
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·July 2, 2025
OSS AXLE
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·July 2, 2025
QUILL SRS
FDA Adverse Event
Other
·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·October 31, 2008