7 results
·
28ms
·
Sources: EU EUDAMED, US FDA
REPL. PISTON FOR TROUTMAN CORNEAL PUNCH
FDA 510(k)
FDA Class 1
·Ophthalmic
MODIFICATION TO: INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE , MODEL 9076
FDA 510(k)
FDA Class 2
·Orthopedic
VERTETRAC
FDA 510(k)
FDA Class 1
·Orthopedic
GORE® TAG® THORACIC ENDOPROSTHESIS
FDA Adverse Event
Death
·W.L. GORE & ASSOCIATES·Product code MIH·July 12, 2015
8800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 14, 2014
PENTA
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMDOULATION·Product code LGW·October 12, 2012
UPHOLD VAGINAL SUPPORT SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·August 10, 2010