Techno Trends

This section presents the latest developments, inventions, and revolutionary technologies that change the face of healthcare.

QuantalX Receives FDA Breakthrough Device Designation for Delphi Stimulator, Revolutionizing Brain Health Diagnosis

QuantalX Neuroscience has announced that its Delphi-MD (Direct Electrophysiological Imaging Device), an advanced neurodiagnostic platform designed for point-of-care use...

Philips Introduces Spectral CT 7500 RT, the World’s First Spectral 4DCT with FDA 510(k) Clearance

Philips has announced the FDA 510(k) clearance for its Spectral CT 7500 RT, the first detector-based spectral 4DCT solution for radiotherapy.  This innovation is set to advance cancer treatment...

Stamford Health Introduces a Groundbreaking AI-Powered Cardiovascular Screening Technology

Stamford Health's Heart & Vascular Institute is set to become the first in Connecticut to implement a new artificial intelligence (AI) tool designed to enhance cardiovascular screening...

Restore Medical Receives Breakthrough Device Designation from FDA for ContraBand™ System to Treat HFrEF Patients

Restore Medical has announced that its ContraBand™ device has received Breakthrough Device Designation from the U.S. Food and Drug Administration (FDA). ...

First-of-Its-Kind Thyroid Ultrasound AI Software from See-Mode Technologies Receives FDA Approval

See-Mode Technologies has announced 510(k) clearance from the U.S. Food and Drug Administration for software designed for thyroid ultrasound analysis and reporting....

FDA Approves SI-BONE's iFuse TORQ TNT Implant System as a Breakthrough Device for Pelvic Fractures

SI-BONE has received FDA 510(k) clearance breakthrough device iFuse TORQ TNT™ Implant System (TNT) for Pelvic Fracture Fixation System....

FDA Grants Breakthrough Device Status to Spryte Medical for Neuro Optical Coherence Tomography Technology

Spryte Medical announces its neuro Optical Coherence Tomography (nOCT) technology, which has received Breakthrough Device designation from the U.S. Food and Drug Administration...

MiRus Introduced First-of-its-kind EUROPA® Posterior Cervical System for Spine Implants

MiRus has received FDA Priority Device Designation for its EUROPA® Posterior Cervical System, which utilizes proprietary rhenium alloys to treat the cervical and upper thoracic spine....

Oticon Medical’s Luanches Novel Device Sentio™ System for Bone Conduction Hearing

Oticon Medical announced clearance of its first active transcutaneous bone conduction hearing system, the Sentio System....

Renata Medical’s First-of-Its-Kind Minima Growth Stent Receives US FDA Approval

Renata Medical  announced that the U.S. Food and Drug Administration (FDA) has approved first-of-its-kind Minima Growth Stent, specifically tailored for neonates, infants, and young children....