16 results
·
18ms
·
Sources: EU EUDAMED, US FDA
DISPOPROPHY
FDA 510(k)
FDA Class 2
·Dental
artegral life
FDA UDI
Merz Dental GmbH·D7091993182·anteriors; shade B1; mould ITM
SET GRI-FILL 3.0
FDA 510(k)
FDA Class 2
·General Hospital
Evis Exera III Duodenovideoscope Olympus TJF-Q190V
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
SPECIFIC DEVICE NOT REPORTED
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JDI·June 18, 2024
EVIS EXERA III DUODENOVIDEOSCOPE
FDA Adverse Event
Injury
·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDT·February 18, 2022
FOXCROSS PTA BALLOON
FDA Adverse Event
Injury
·ABBOTT VASCULAR·Product code LIT·February 27, 2013
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 7, 2011
CONSULTA CRT-D
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·August 8, 2014
INFUSE(R) Bone Graft, SMALL KIT, REF 7510200, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic
FDA Recall
Terminated
·Medtronic Sofamor Danek USA Inc·Product code NEK·May 28, 2013
INFUSE(R) Bone Graft, LARGE KIT, REF 7510600, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic
FDA Recall
Terminated
·Medtronic Sofamor Danek USA Inc·Product code NEK·May 28, 2013
INFUSE(R) Bone Graft, MEDIUM KIT, REF 7510400, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic
FDA Recall
Terminated
·Medtronic Sofamor Danek USA Inc·Product code NEK·May 28, 2013
INFUSE(R) Bone Graft, SMALL KIT, REF 7510200AUS, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic
FDA Recall
Terminated
·Medtronic Sofamor Danek USA Inc·Product code NEK·May 28, 2013
INFUSE(R) Bone Graft, MEDIUM KIT, REF 7510400AUS, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic
FDA Recall
Terminated
·Medtronic Sofamor Danek USA Inc·Product code NEK·May 28, 2013
INFUSE(R) Bone Graft, LARGE II KIT, REF 7510800AUS, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic
FDA Recall
Terminated
·Medtronic Sofamor Danek USA Inc·Product code NEK·May 28, 2013
INFUSE(R) Bone Graft,LARGE II KIT, REF 7510800, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic
FDA Recall
Terminated
·Medtronic Sofamor Danek USA Inc·Product code NEK·May 28, 2013