14 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Endo Quickconnect Olympus Scope Port Connector, Endo Quickconnect Pentax Scope Port Connector
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
SKINTACT RADIOTRANSPARENT MULTIFUNCTION ELECTRODES
FDA 510(k)
FDA Class 3
·Cardiovascular
H & L (NIBP) BLOOD PRESSURE MONITOR, MODEL HL888EM
FDA 510(k)
FDA Class 2
·Cardiovascular
MICRO SCREW 1.2MM X 3MM
FDA Adverse Event
Injury
·OSTEOMED, LLC·Product code DZL·August 24, 2022
1.6MM X 5MM SCREW
FDA Adverse Event
Injury
·OSTEOMED, LLC·Product code DZL·August 24, 2022
1.6MM X 4MM SCREW
FDA Adverse Event
Injury
·OSTEOMED, LLC·Product code DZL·August 24, 2022
1.6MM X 4MM SCREW
FDA Adverse Event
Injury
·OSTEOMED, LLC·Product code DZL·August 24, 2022
1.6MM X 4MM SCREW
FDA Adverse Event
Injury
·OSTEOMED, LLC·Product code DZL·August 24, 2022
1.6MM, STRAIGHT PLATE, 18MM
FDA Adverse Event
Injury
·OSTEOMED, LLC·Product code HRS·August 24, 2022
1.6MM, STRAIGHT PLATE, 18MM
FDA Adverse Event
Injury
·OSTEOMED, LLC·Product code HRS·August 24, 2022
ACCENT DR RF
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC. CRMD·Product code DXY·January 13, 2014
WALLFLEX? COLONIC
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - GALWAY·Product code MQR·June 3, 2013
WALLFLEX BILIARY RX PARTIALLY-COVERED STENT SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - GALWAY·Product code FGE·June 28, 2011
OEC 6800 Miniview, Image-intensified fluoroscopic x-ray system used during diagnostic, surgical and interventional procedures. Designed to provide the physician with general fluoroscopic visualization of the patient including but not limited to surgical orthopedic and extremity imagine. The device is not intended for whole-body pediatric imaging.
FDA Enforcement
Class I
·Terminated·GE OEC Medical Systems, Inc·August 1, 2012