Technology

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Conavi Medical Receives FDA Clearance for Feature Expansion on Foresight Intracardiac Echocardiography System
Technology | Ultrasound Intra-cardiac Echo (ICE) | May 01, 2017

Conavi Medical Inc. announced 510(k) clearance from the U.S. Food and Drug Administration (FDA)...

Resolute Onyx DES, drug eluting stent, medtronic, gains FDA approval
Technology | Stents Drug Eluting | May 01, 2017

May 1, 2017 — The U.S.

Physio-Control Launches HeartSine samaritan PAD 360P Automated External Defibrillator in United States
Technology | Defibrillator Monitors | April 24, 2017

Physio-Control announced April 19 that the company’s HeartSine samaritan PAD 360P (SAM 360P)...

FDA Clears Siemens Somatom go. CT platform
Technology | Computed Tomography (CT) | April 11, 2017

The U.S. Food and Drug Administration (FDA) has cleared the Somatom go. computed tomography (CT...

Biotronik, Edora series, pacemakers, CRT-Ps
Technology | Cardiac Resynchronization Therapy Devices (CRT) | March 23, 2017

March 23, 2017 — Biotronik announced the European launch of the Edora series, its smallest...

Aegis Medical Innovations, Sierra Ligation System, U.S. clinical trial, FDA approval, LAA occluder
Technology | Left Atrial Appendage (LAA) Occluders | March 22, 2017

Aegis Medical Innovations Inc. announced that it has received Investigational Device Exemption...

Technology | Guidewires | March 20, 2017

March 20, 2017 — Teleflex Inc. recently announced 510(k) clearance by the U.S.

Agfa HealthCare, Enterprise Imaging for Cardiology, ACC.17, IBM Watson Health
Technology | Enterprise Imaging | March 20, 2017

March 20, 2017 — Agfa HealthCare announced the release a new version of its...

Toshiba Medical, Aplio i900 cardiovascular ultrasound, FDA clearance, ACC 2017, RSNA 2017
Technology | Cardiovascular Ultrasound | March 20, 2017

March 20, 2017 — Cardiologists can now access the advanced...

Medtronic, Reveal LINQ ICM, insertable cardiac monitor, FDA clearance, TruRhythm Detection
Technology | Implantable Cardiac Monitor (ICM) | March 15, 2017

Medtronic plc announced U.S. Food and Drug Administration (FDA) 510(k) clearance for its Reveal...

Siemens Healthineers, Artis pheno angiography system, FDA approval, ACC 2017, RSNA 2017
Technology | Angiography | March 15, 2017

The U.S. Food and Drug Administration (FDA) has cleared the Artis pheno robotic C-arm...

Melody transcatheter pulmonary valve, FDA expands indication, Melody for use in replacing failed surgical valves
Technology | Heart Valve Technology | March 14, 2017

March 14, 2017 — The United States Food and Drug Administration (FDA) has expanded use of the...

Zoll, Hospital Wearable Defibrillator, HWD, FDA premarket approval
Technology | Defibrillator Monitors | March 10, 2017

Zoll Medical Corp. announced that the company’s Hospital Wearable Defibrillator (HWD) has been...

RaySafe i3 dosimeter, real-time radiation dose monitoring, wearable, RSNA 2017

Image courtesy of Unfors RaySafe

Technology | Radiation Dose Management | March 07, 2017

March 7, 2017 — Unfors RaySafe recently introduced the RaySafe i3, to its suite of real-time...

ON Semiconductor, KAF-09001 image sensor, video imaging, digital radiography, angiography, radiographic fluoroscopy, R/F systems
Technology | Angiography | March 06, 2017

ON Semiconductor announced the release of a new CCD image sensor that enables video imaging...

tryton side branch stent, dedicated coronary side branch stent

The Tryton Side Branch Stent is deployed in the side branch artery using a standard single wire balloon-expandable stent delivery system. A conventional drug eluting stent is then placed in the main vessel.

Technology | Stents Bifurcation | March 06, 2017

March 6, 2017 – The U.S.

Philips, Azurion platform, angiography, interventional lab, global launch
Technology | Angiography | March 03, 2017

Philips recently announced the global launch of Azurion, its next-generation image-guided...

Teleflex, FDA 510k clearance, TrapLiner Catheter, U.S. launch
Technology | Catheters | March 02, 2017

Teleflex Inc. has announced 510(k) clearance by the U.S. Food and Drug Administration (FDA) and...

CeloNova Cobra Pzf stent
Technology | Stents | March 02, 2017

March 2, 2017 — The U.S. Food and Drug Administration (FDA) cleared CeloNova BioSciences Inc.

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