Olympus Wins FDA Nod for Advanced Endoscopes
Olympus has received FDA 510(k) clearance for its EZ1500 series endoscopes, featuring Extended Depth of Field (EDOF) technology—the company’s most advanced imaging yet for gastrointestinal
Olympus has received FDA 510(k) clearance for its EZ1500 series endoscopes, featuring Extended Depth of Field (EDOF) technology—the company’s most advanced imaging yet for gastrointestinal
NeuroPace has released preliminary one-year results from its Nautilus clinical trial, assessing its RNS System for idiopathic generalized epilepsy (IGE). While the study did not
Medtronic’s next-generation Nellcor pulse oximetry technology has been accepted into the FDA’s Safer Technologies Program (STeP), a designation aimed at accelerating safer medical device development.
BD has announced XTRACT, a new U.S.-based patient registry to evaluate real-world outcomes of its Rotarex atherectomy system for peripheral artery disease (PAD). The single-arm,
Distalmotion has received FDA 510(k) clearance for using its Dexter surgical robot in adult gallbladder removal (cholecystectomy), marking its second U.S. indication following inguinal hernia
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