16 results
·
26ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
SMITH & NEPHEW 6.5MM AND 8.0MM CANNULATED SCREWS
FDA 510(k)
FDA Class 2
·Orthopedic
INRATIO
FDA Adverse Event
Malfunction
·HEMOSENSE, INC.·Product code JPA·March 30, 2007
INRATIO
FDA Adverse Event
Malfunction
·HEMOSENSE, INC.·Product code JPA·March 16, 2007
TRAATEK COTTONOID PATTIES
FDA 510(k)
FDA Class 2
·Neurology
LA JOIE
FDA 510(k)
FDA Class 1
·Obstetrics/Gynecology
VERTE-STACK K030736, K041197
FDA Adverse Event
Death
·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code MQP·January 4, 2019
UNKNOWN NOTTINGHAM SHOULDER
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code MBF·May 17, 2017
INRATIO
FDA Adverse Event
Malfunction
·HEMOSENSE, INC.·Product code JPA·March 28, 2007
INRATIO
FDA Adverse Event
Malfunction
·HEMOSENSE, INC.·Product code JPA·February 22, 2007
SINGLE USE ASPIRATION NEEDLE
FDA Adverse Event
Malfunction
·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code GAA·March 29, 2013
MICROPLEX COMPASS COMPLEX COIL (MCS)
FDA Adverse Event
Malfunction
·MICROVENTION, INC.·Product code HCG·June 11, 2008
ANIMAS INSULIN INFUSION CARTRIDGE
FDA Adverse Event
Malfunction
·ANIMAS CORP·Product code LZG·April 8, 2011
INRATIO
FDA Adverse Event
Malfunction
·HEMOSENSE, INC.·Product code JPA·February 23, 2007
COMPREHENSIVE SHOULDER SYSTEM MODULAR HEAD - VARIABLE OFFSET 42MM X 18MM X 46MM
FDA Adverse Event
Malfunction
·BIOMET ORTHOPEDICS·Product code HSD·October 19, 2016
FRESENIUS COM.TEC AUTOMATED CELL SEPARATOR
FDA Adverse Event
Death
·FRESENIUS HEMOCARE GMBH·Product code LKN·August 21, 2023
FRESENIUS COM.TEC AUTOMATED CELL SEPARATOR
FDA Adverse Event
Death
·FRESENIUS HEMOCARE GMBH·Product code LKN·August 21, 2023