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Recent from Imaging
GE Announces First U.S. Install of General Purpose Digital SPECT/CT
Global Contrast Media Injectors Market to Reach $1.8 Billion by 2022
Computed Tomography (CT)
Magnetic Resonance Imaging (MRI)
Recent from Cath Lab
National Hospital System Uses Enterprise Approach to Assess PCI Bleeding Risks
Final Three-Year ORBIT II Atherectomy Study Results Shared
Intravascular imaging systems
Peripheral Artery Disease
Recent from EP Lab
Poor Warfarin Management Increases Kidney Failure Risk for Afib Patients
Acutus Medical Receives CE Mark for AcQMap 3-D Imaging and Mapping System
Implantable cardioverter defibrillators (ICD)
Cardiac resynchronization therapy devices (CRT)
Leads, implantable devices
Recent from Structural Heart
First Central Pennsylvania Patients Receive New Aortic Valve Reconstruction Procedures
AtriCure Receives FDA Clearance for New AtriClip Device
Heart Valve Repair
Left atrial appendage (LAA) occluders
Structural heart occluders/closure devices
Recent from Information Diagnostics
New Case Series Examines CardioMEMS in Single Ventricle Fontan Anatomy
Heart Monitoring Suggested for All Breast Cancer Patients Undergoing Herceptin Treatment
Recent from Information Technology
SCAI Eye Exams for Interventional Cardiologists Helps Track Radiation Exposure
FTC Creates Compliance Tool for Mobile Health App Developers
Clinical decision support
Aptus Endosystems Inc.
777 N. Pastoria Avenue
(408) 530 - 9050
(408) 530 - 9051
Endovascular Aortic Repair
Heli-FX image courtesy of Aptus Endosystems
Endovascular Aortic Repair
July 02, 2015
Medtronic Acquires Aptus Endosystems
Medtronic plc announced it has acquired the assets of Aptus Endosystems Inc., a privately held medical device company...
November 17, 2014
Late-Breaking Clinical Trial Results Announced at VIVA 2014
VIVA Physicians, a not-for-profit organization in the field of vascular medicine and intervention, announced late-...
June 24, 2013
FDA Clears Heli-FX Guide Designed to Treat Wide Neck Abdominal Aortic Aneurysms
Aptus Endosystems Inc. announced that it received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for...
October 04, 2012
Aptus Endosystems Receives FDA Clearance For Thoracic-Length HeliFX Aortic Securement System
Aptus Endosystems Inc. announced it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for...
July 09, 2012
Aptus Endosystems Completes $25 Million in Financing
July 9, 2012 — Endosystems Inc., a medical device company developing technology for endovascular aneurysm repair (EVAR...
February 15, 2012
Aptus Endosystems Initiates the ANCHOR Post-Market Registry
February 16, 2012 — Aptus Endosystems, a company developing advanced technology for endovascular aneurysm repair (EVAR...
December 14, 2011
New Aortic Aneurysm Repair Technology From Aptus Cleared by FDA
December 14, 2011 — Aptus Endosystems Inc. announced it received 510(k) clearance from the U.S. Food and Drug...
November 23, 2011
FDA Clears Endostaple System to Repair Leaking Stent Grafts
November 23, 2011 – The U.S. Food and Drug Administration (FDA) allowed marketing of the first system that can repair...
May 24, 2011
Aptus Endosystems Inc. Receives CE Mark for the Aptus EndoStapling System
May 24, 2011 — Aptus Endosystems Inc., a medical device company developing advanced technology for endovascular...
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