10 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
VARIABLE ANGLE, HEXALOBE SCREW (TI-6AI-4V ELI)
FDA Adverse Event
Injury
·ALPHATEC SPINE INC·Product code KWQ·June 24, 2019
MECTALIF ANTERIOR STAND-ALONE PLATE FLUSH H.12 MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code OVD·March 29, 2018
BD US CATHENA 22GX1.00IN STRAIGHT BC
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FOZ·January 8, 2025
4.0MM SELF-TAPPING, HEXALOBE SCREW, 14MM (TI-6AI-4V ELI)
FDA Adverse Event
Malfunction
·ALPHATEC SPINE INC·Product code KWQ·June 26, 2017
HS III PROXIMAL SEAL SYSTEM 3.8MM
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR, LLC·Product code DXC·May 15, 2013
CAPSURE SENSE
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·June 14, 2011
SENSOR ENLITE
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OZO·October 2, 2015
ALIF SCREWDRIVER UNIVERSAL JOINT
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code LXH·January 15, 2016
MECTALIF ANTERIOR SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code OVD·May 6, 2025
MECTALIF ANTERIOR TI-PEEK CAGE
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code OVD·January 4, 2018