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MassDevice10h
Ambu wins FDA clearance for first single-use cysto-nephroscope
Ambu has received expanded FDA 510(k) clearance for its aScope 5 Cysto HD, making it the first single-use flexible ...
IBN Coverage: HeartBeam (NASDAQ: BEAT) Earns FDA Clearance for First Cable-Free ECG System for Arrhythmia Detection
This article was published by IBN, a multifaceted communications organization engaged in connecting public companies to the ...
GlobalData on MSN1d
Exo lands FDA clearance for two AI lung disease ultrasound apps
According to Exo, the AI apps for its ultrasound device to detect two common lung conditions are the first of their kind to ...
MassDevice2d
FDA grants expanded clearance for Levita Magnetics surgical robot
Levita Magnetics announced today that it received expanded FDA 510(k) clearance for its MARS (magnetic-assisted robotic ...
TMCnet2d
Exo Launches a New Era in Disease Diagnosis with the First FDA-cleared Ultrasound AI for Detection of Pleural Effusion and Consolidation/Atelectasis
Exo (pronounced "echo"), the leader in AI-powered, accessible medical imaging, is transforming lung disease diagnosis with ...
Pharmabiz18h
Expanding Innovations receives US FDA 510(k) clearance for its spinal fixation platform N-GAGE Lumbar Plate System
Expanding Innovations receives US FDA 510(k) clearance for its spinal fixation platform N-GAGE Lumbar Plate System: Mountain View, California Friday, June 20, 2025, 13:00 Hrs [IST ...
Biomednewsbreaks - Heartbeam Inc. (NASDAQ: BEAT) Earns FDA Clearance For First Cable-Free ECG System For Arrhythmia Detection
HeartBeam (NASDAQ: BEAT) announced it has received FDA 510(k) clearance for its flagship ECG system, a first-of-its-kind, credi ...
Endovascular Today4d
Inquis’ Aventus Thrombectomy System Cleared to Treat PE - Clone
Inquis Medical announced that its Aventus mechanical thrombectomy system has received FDA 510(k) clearance for an expanded ...
Endovascular Today3d
Crossroads Neurovascular’s Path Balloon Guide Catheter Cleared by FDA
Crossroads Neurovascular, Inc. announced FDA 510(k) clearance for the company’s Path balloon guide catheter (BGC) for neurov ...
Pharmabiz6d
Neurent Medical receives US FDA’s 510(k) clearance for its next generation Neuromark system
Neurent Medical receives US FDA’s 510(k) clearance for its next generation Neuromark system: Galway, Ireland Saturday, June 14, 2025, 17:00 Hrs [IST] Galway-headquartered Neuren ...