Techno Trends
The most recent inventions, innovations, and ground-breaking technologies that are revolutionizing the healthcare landscape are presented to you in this section.
US FDA Approves Werfen's New Aptiva® Reagents for Antiphospholipid Syndrome
Werfen has received 510(k) clearance from the US Food and Drug Administration (FDA) for its Aptiva® Antiphospholipid Syndrome (APS) Immunoglobulin G (IgG) and Immunoglobulin M (IgM) Reagents....
FDA Grants Breakthrough Device Designation to AccurKardia's AK+ Guard™ for AI-powered Hyperkalemia Detection
AccurKardia has achieved a significant milestone with the U.S. Food and Drug Administration (FDA) granting Breakthrough Device Designation for its AK+ Guard™ hyperkalemia detection software. This innovative, AI-driven solution leverages Lead I ECG data to assist in identifying moderate to severe episodes...
FDA Approves Ventris Medical's First-of-Its-Kind 510(k) Clearance for Backpack® Bone Graft System.
Ventris Medical has announced that the United States Food and Drug Administration (FDA) has granted 510(k) clearance for its Backpack® Porous Biologic Scaffold (K240765). Backpack® introduces a novel category of biomaterials aimed at enhancing cell proliferation and bone formation, specifically designed for use in orthopaedic and spinal fusion procedures. ...
Dexcom Innovates Groundbreaking First Generative AI Platform in Glucose Biosensing
Dexcom has announced the launch of its new GenAI platform, making it the first continuous glucose monitoring (CGM) company to integrate Generative AI into glucose biosensing technology....
FDA Approves R3 Vascular's Novel MAGNITUDE® Bioresorbable Scaffold for Below-the-Knee PAD
R3 Vascular has received approval from the U.S. Food and Drug Administration to start its ELITE-BTK pivotal trial. This trial will test the next generation of the company’s drug-eluting bioresorbable scaffold...
FDA Approves GT Metabolic's First-of-Its-Kind MagDI™ System for Duodeno-Ileal Anastomosis
GT Metabolic Solutions has announced that the U.S. Food and Drug Administration has cleared its MagDI™ System for side-to-side duodeno-ileal (DI) anastomosis....
Invenio Imaging Receives FDA Breakthrough Designation for AI-Powered Lung Biopsy Analysis Module
Invenio Imaging has announced that the U.S. FDA has granted Breakthrough Device Designation for its NIO® Lung Cancer Reveal image analysis module....
Adona Medical Introduces First Human Trial of Its Novel Interatrial Shunt for Heart Failure Patients
Adona Medical focused on advancing heart failure treatments, has successfully carried out the first human use of its novel interatrial shunt device....
CroiValve Introduces First Implant of Minimally Invasive Device for Tricuspid Regurgitation
CroíValve, specialising in the development of transcatheter solutions, has announced the first patient treatment using its DUO™ System in the TANDEM II Early Feasibility Study in the United States....
Cook Medical Unveils PillSense™ a Breakthrough Device for Advanced Blood Sensing Technology
Cook Medical has introduced the distribution of the PillSense™ GI Bleed Detection System in the United States. This innovative device can detect upper gastrointestinal (GI) bleeding in patients within 10 minutes...