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IceCure Receives FDA Clearance for Expanded Indications of Cryoablation Technology and Approval of MultiSense System

January 7, 2020—IceCure Medical Ltd. announced FDA clearance of expanded indications for the company’s cryoablation technology.

FDA Clears Centerline's IOPS Intraoperative Positioning System

July 10, 2019—Centerline Biomedical, Inc. announced that the company has received FDA 510(k) clearance to market its IOPS intraoperative positioning system.

Bentley Acquires the GoBack Catheter From Upstream Peripheral Technologies

September 13, 2022—Bentley, based in Hechingen, Germany, announced it has acquired the rights of the GoBack catheter from Upstream Peripheral Technologies, which is headquartered in Caesarea, Israel.

FDA Clears Medical Ingenuities’ PH Band Radial Artery Occlusion Device

December 9, 2020—Medical Ingenuities’ radial artery occlusion device, PH Band, has received FDA 510(k) clearance.

Vena Medical’s Balloon Distal Access Catheter Investigated in Canada With First-Ever Procedures

August 16, 2022—Vena Medical, a Canada-based developer of neurovascular devices, announced the successful treatment of the first five patients in the world using the Vena balloon distal access catheter (BDAC) at London Health Sciences Centre (LHSC) University Hospital in London, Ontario, and The Ottawa Hospital (TOH) in Ottawa, Ontario, Canada.

Rapid Medical Receives Funding to Advance Commercialization of Stroke Treatment Devices

July 17, 2017—Rapid Medical, an Israel-based company focused on the development of neurovascular interventional devices, announced that it has completed a Series B financing of $9 million to advance the commercialization of the company's minimally invasive stroke treatment and prevention products, the Tigertriever revascularization device and the Comaneci adjustable remodeling mesh.

FDA Clears Rex Medical's Revolution Peripheral Atherectomy System

September 12, 2019—Rex Medical, LP announced that it has received FDA 510(k) clearance for the Revolution peripheral atherectomy system.

Ra Medical Announces Progress of the Next-Generation DABRA Excimer Laser System

June 29, 2021—Ra Medical Systems, Inc. announced that enrollment in the pivotal atherectomy clinical trial with its DABRA excimer laser system is now at 62 patients, including 42 patients enrolled since the beginning of 2021.

2-Year ATTRACT Data: Anticoagulation Alone Best for Most DVT; PCDT Benefits Seen in Certain Iliofemoral Patients

March 6, 2017—The much-anticipated 2-year results from the ATTRACT study were presented by Suresh Vedantham, MD, FSIR, on behalf of the trial’s investigators, at the 2017 Society of Interventional Radiology (SIR) Annual Scientific Meeting.

GE HealthCare CleaRecon DL for CBCT Imaging Launched in United States and Europe

May 21, 2025—GE HealthCare recently announced the launch of CleaRecon DL in the United States and European Union.

InspireMD Announces PIs for C-GUARDIANS II Trial Evaluating the SwitchGuard Neuroprotection System

February 12, 2024—InspireMD, Inc. named Patrick Geraghty, MD, and Patrick Muck, MD, as the lead Principal Investigators (PIs) for the company’s upcoming C-GUARDIANS II clinical trial for the SwitchGuard neuroprotection system (NPS).  According to the company, the C-GUARDIANS II study will aim to advance clearance of SwitchGuard NPS and associated tools, which are designed to allow the treating physician to reverse cerebral blood flow during a transcarotid artery revascularization procedure, preventing embolic debris generated during the procedure from traveling to the brain by passing the blood through the filter enclosed within the SwitchGuard before returning it to the patient to minimize blood loss.

Percutaneous AV Fistula Creation Systems Gain FDA Marketing Authorization

June 22, 2018—The US Food and Drug Administration has announced the marketing authorization of two systems designed to percutaneously create arteriovenous (AV) fistulas in hemodialysis patients.

Zoll to Acquire Philips' InnerCool Business

November 17, 2014—Zoll Medical Corporation, an Asahi Kasei Group company, announced that it has signed an agreement to purchase substantially all of the assets of Royal Philips Electronics’ InnerCool temperature management business.

Siemens Healthineers Naeotom Alpha Photon-Counting CT Technology Cleared by FDA

September 30, 2021—Siemens Healthineers announced FDA 510(k) clearance of the Naeotom Alpha, a photon-counting CT.