Techno Trends
The most recent inventions, innovations, and ground-breaking technologies that are revolutionizing the healthcare landscape are presented to you in this section.
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)....
MeMed Receives FDA Approval to MeMed BV Flex™ Breakthrough Device Designation for Capillary Blood Test
MeMed has been granted Breakthrough Device Designation (BDD) by the U.S. Food and Drug Administration for its MeMed BV Flex™ diagnostic test....
Airiver Medical Secures FDA Breakthrough Device Status for Novel Pulmonary Balloon
Airiver Medical has announced that its Pulmonary Drug-Coated Balloon (DCB) has received Breakthrough Device designation from the U.S. Food and Drug Administration....
Vesalio Introduces New Neurovascular Devices: NeVa™ VS and NeVa™ 3.0 mm Thrombectomy System
Vesalio, a global innovator in vascular interventions, has launched two new neurovascular devices in Europe following CE Mark certification: the NeVa™ VS for treating cerebral vasospasm after aneurysmal...
FDA Grants Breakthrough Device Status to NG Biotech and Hardy Diagnostics for Two Rapid Pathogen Tests
NG Biotech, in collaboration with Hardy Diagnostics, has received Breakthrough Device Designations from the U.S. Food and Drug Administration (FDA) for two innovative diagnostic tests: NG-TEST® Candida auris and NG-TEST® Acineto-5®....
