The Direxion Torqueable Microcatheter-a microcatheter for shrinking tumors or blocking aneurysms-has won FDA and CE Mark approval, Boston Scientific recently announced. The FDA granted the Direxion a 510(k) clearance because it retains ...
Tags: Boston Scientific Microcatheter, FDA Approval, Direxion a 510(k)
Medical device company EndoStim has announced that Argentina's National Administration of Drugs, Food and Medical Technology (ANMAT) approved its lower esophageal sphincter (LES) stimulation system for gastroesophageal reflux disease ...
Tags: Medical device, Gerd Treatment
EndoStim has received CE mark approval for its LES Stimulation system, designed to treat gastro-esophageal reflux disease (GERD) and eliminate the need for daily proton pump inhibitor (PPI) medication. By using low energy electrical ...
Medical device company Nexstim in Finland,has obtained CE mark approval for its non-invasive Navigated Brain therapy(NBT)system. The system featuring MRI-based navigation allows users to visualize the electric field inside the patient's ...
Tags: medical device, Nexstim, NBT system, brain
NeuroSigma has obtained CE mark approval for its external Trigeminal Nerve Stimulation (eTNS) system, Monarch, designed for the treatment of epilepsy and major depressive disorder in adults and children of 9 years and older. The eTNS ...
Tags: NeuroSigma, eTNS, FDA