Techno Trends
The most recent inventions, innovations, and ground-breaking technologies that are revolutionizing the healthcare landscape are presented to you in this section.
Hyperfine Brings First-of-its-Kind Portable MRI Technology to AIIMS New Delhi
Hyperfine, Inc. and the All India Institute of Medical Sciences, New Delhi, have announced the clinical deployment of the Swoop® portable MRI system, making AIIMS the first hospital in India to use bedside MRI technology for routine patient care....
Pixee Medical Gains FDA Clearance for Novel Knee+ NexSight AR System
Pixee Medical has received U.S. FDA 510(k) clearance for Knee+ NexSight, its next-generation augmented reality navigation system for total knee arthroplasty (TKA)....
Philips Receives FDA Approval for Novel Rembra Imaging Technology
Philips has received 510(k) clearance from the US Food and Drug Administration for its Rembra platform, which includes the Rembra CT, Rembra RT, and Areta RT systems....
Agitated Solutions Secures CE Mark for Orbis™ Microbubble Generator
Agitated Solutions has secured CE Mark approval in the European Union for its Orbis™ Microbubble Generator, allowing the company to market the device across EU countries....
Medtronic Receives First-of-its-Kind FDA Approval for OmniaSecure™ Defibrillation Lead
Medtronic has received expanded U.S. Food and Drug Administration (FDA) approval for its OmniaSecure™ defibrillation lead, allowing its use for conduction system pacing (CSP) in the left bundle branch (LBB) area...
Baebies Receives First-of-its-Kind FDA Clearance and CLIA Waiver for FINDER® Flu A&B/SARS-CoV-2 Test
Baebies has announced that its FINDER® Flu A&B/SARS-CoV-2 Test has received both U.S. Food and Drug Administration (FDA) 510(k) clearance and CLIA waiver approval....
InVera Medical Receives FDA Clearance for InVera Infusion Device for Chronic Venous Disease
InVera Medical has received U.S. Food and Drug Administration (FDA) 510(k) clearance for its InVera Infusion Device, a novel non-thermal catheter designed to improve the delivery of sclerosant therapy in diseased leg veins, including varicose veins....
Etiometry Receives First FDA Clearance for Automated Hospital-Specific Cardiogenic Shock Classification Tool
Etiometry, a provider of AI-driven clinical intelligence solutions, has received U.S. Food and Drug Administration (FDA) clearance (K254066) for its Cardiogenic Shock Tool, the first system authorised to automate hospital-specific...
Endo Tools Therapeutics Receives FDA Clearance for Next-Generation endomina® EZFuse System
Endo Tools Therapeutics (ETT) has announced that the U.S. Food and Drug Administration (FDA) has granted 510(k) clearance for its next-generation endomina® EZFuse system....
SetPoint Medical Performs FDA Approved First SetPoint® System Procedure
SetPoint Medical has completed the first procedure in Texas using the FDA-approved SetPoint System®, an implantable neuroimmune modulation device for adults with moderately to severely active rheumatoid arthritis (RA)....
