11 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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QUICKSCREEN ONE STEP OPIATE SCREENING TEST (9080)
FDA 510(k)
FDA Class 2
·Clinical Toxicology
NEXGEN COMPLETE KNEE SOLUTION LPS-FLEX AND KNEE GENDER SOLUTIONS FEMALE (GSF) POROUS FEMORAL COMPONENTS
FDA 510(k)
FDA Class 2
·Orthopedic
RMC KNEE METAL SHOE TIBIAL COMPONENTS
FDA 510(k)
FDA Class 2
·Orthopedic
SS COMPRESSION HIP SCREW LAG SCREW
FDA Adverse Event
Injury
·BIOMET TRAUMA·Product code KTT·September 19, 2016
IBP ELBOW INTERLOK FINISH ULNAR COMPONENT STANDARD LEFT
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDB·June 14, 2017
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDB·February 9, 2017
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDB·March 2, 2017
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDB·February 9, 2017
TENSION FREE VAGINAL TAPE
FDA Adverse Event
Injury
·ETHICON, INC.·Product code OTN·February 21, 2013
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·January 13, 2011
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·August 1, 2014