Medtech

CIRCA Scientific's PeriCross™ Epicardial Access Kit Receives FDA 510(k) Clearance

CIRCA Scientific receives FDA 510(k) clearance for the PeriCross™ Epicardial Access Kit, a novel tine-based system designed to support controlled and efficient subxiphoid access to the pericardial space....Read more

25th April, 2025


Dr. Kingsley R. Chin and KIC Ventures Celebrate 25 Years of Surgeon-Led Innovation

From the OR to the boardroom, a growing wave of entrepreneurial physicians is reshaping the future of spine surgery and healthcare innovation...Read more

25th April, 2025


Center for Better Aging Extends Chicago Testing, Diagnostic Access

St. Bernard Hospital CT/Mammography Suite Addresses South Side's Health Risks ...Read more

24th April, 2025


Baebies Receives FDA Breakthrough Device Designation for First Point-of-Care Heparin Monitoring Test

FINDER® platform enables rapid, low-volume Anti-Factor Xa testing, transforming anticoagulation care at the bedside....Read more

24th April, 2025


BD Launches First-of-its-Kind Bioabsorbable Mesh for Umbilical Hernia Repair

Innovative mesh aims to improve patient outcomes by naturally absorbing into the body post-surgery. ...Read more

24th April, 2025


Clarivate Unveils DRG Commercial Analytics 360 for Medtech

New solution provides integrated provider intelligence and real-world data to optimize targeting, strategic planning and patient access across commercial organizations...Read more

23rd April, 2025


Theranica's Nerivio® Wearable Migraine Device Secures Coverage from Major U.S. Health Insurer

The policy expands access to this effective, non-drug treatment for members as young as 8 years old who are diagnosed with migraine ...Read more

23rd April, 2025


Laxco Launches Accuva LEAP – Next-Gen Imaging System for Advanced Research

The innovative platform sets a new benchmark in high-resolution imaging tailored for cutting-edge scientific exploration....Read more

23rd April, 2025


USA: Minder® Becomes First FDA-Approved Implantable Continuous EEG MonitorUSA: Minder® Becomes First FDA-Approved Implantable Continuous EEG Monitor

The FDA has granted authorisation for Minder under its De Novo pathway creating a new classification of device, allowing for marketing and sale of the device in the US for patients with drug resistant epilepsy...Read more

23rd April, 2025


U.S.: Sight Sciences to Debut OMNI® Edge Surgical System at 2025 ASCRS Annual Meeting

New system features higher viscoelastic capacity and TruSync™ technology, engineered to safely synchronize surgical control and precision in implant-free, comprehensive MIGS ...Read more

22nd April, 2025


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