23 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
PENTAX
FDA Adverse Event
Injury
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·March 5, 2021
PENTAX
FDA Adverse Event
Injury
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·March 5, 2021
SM104 MSERIES W5TH
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FPO·February 14, 2012
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·November 28, 2020
M2A-MAGNUM MOD HD
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·May 15, 2017
SORBAFIX ENHANCED
FDA Adverse Event
Injury
·DAVOL INC., SUB. C.R. BARD, INC.·Product code GDW·March 12, 2013
OT ULTRA2 METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·March 8, 2011
PERV. VENT. LINEAR BIPOLAR
FDA Adverse Event
Injury
·TELECTRONICS PACING SYSTEMS·Product code DTB·March 10, 2008
M2A-MAGNUM 42-50MM TPR INSRT-6
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·May 15, 2017
OSS POROUS COATED BOWED IM STEM W/SCREW
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·May 5, 2017
OSS AXLE
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·May 5, 2017
OSS POROUS COATED BOWED IM STEM W/SCREW
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·May 5, 2017
OSS FEMORAL BUSHINGS
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·May 5, 2017
OSS 16MM TIBIAL BEARING
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·May 5, 2017
OSS TIBIAL BUSHING
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·May 5, 2017
OSS-K 67 MM MODULAR POROUS COATED W/PLUG TIBIAL BASE
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·May 5, 2017
OSS POROUS COATED IM STEM W/SCREW - 11.5 MM X 90 MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·May 5, 2017
OSS LOCKING PIN
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·May 5, 2017
OSS SEGMENTAL FEMORAL - LEFT 7 CM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·May 5, 2017
SYRINGE 50ML LL
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·June 8, 2021