10 results
·
24ms
·
Sources: EU EUDAMED, US FDA
BIOTHERM
FDA 510(k)
FDA Class 2
·Physical Medicine
Peridot-PT Anterior Cervical Intervertebral body fusion System; Peridot-PT Intervertebral body fusion system; The Peridot-TD Anterior Cervical Intervertebral body fusion system; The Peridot-TD Intervertebral body fusion system
FDA 510(k)
FDA Class 2
·Orthopedic
AMPCO KIDNEY DIALYSIS TRAY
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·May 27, 2014
TAXUS¿ ELEMENT¿
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·November 15, 2012
CG COMPOSITE RING
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES, INC.·Product code KRH·September 8, 2010
TALENT OCCLUDER
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·November 11, 2015
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HRS·November 7, 2016
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HRS·November 7, 2016
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HRS·November 7, 2016