9 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
DynaNail Mini
FDA 510(k)
FDA Class 2
·Orthopedic
B-D 60 ML SYRINGE LUER-LOK TIP
FDA Adverse Event
Malfunction
·B-D·Product code FMF·September 23, 2016
BODYTOM NL 4000
FDA 510(k)
FDA Class 2
·Radiology
AMS ELEVATE ANTERIOR & APICAL PROLAPSE REPAIR SYSTEM WITH INTEPRO LITE
FDA 510(k)
FDA Class 3
·Obstetrics/Gynecology
LUER LOK TIP 60 ML SYRINGE
FDA Adverse Event
Other
·BECTON DICKINSON & CO.·Product code FMF·December 2, 2016
5.5MM/6.0MM TI TAPERED ROD 500MM
FDA Adverse Event
Injury
·SYNTHES USA·Product code NKB·June 21, 2013
TERUMO PERFUSION SYSTEM 8000
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code JOR·July 5, 2011
DELTA SHUNT KIT, SMALL PERFORMANCE LEVEL 1.5
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROSURGERY·Product code JXG·September 25, 2008
INVICTUS SPINAL FIXATION SYSTEM
FDA Adverse Event
Injury
·ALPHATEC SPINE, INC.·Product code NKB·April 30, 2025