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Diverging trajectories of trust in healthcare and on-line information seeking: what’s next with LLMs

Diverging trajectories of trust in healthcare and on-line information seeking: what’s next with LLMs

February 1, 2026February 1, 2026
Weekly Roundup – January 31, 2026

Weekly Roundup – January 31, 2026

January 31, 2026February 1, 2026
Embedding clinical intelligence to help close care gaps

Embedding clinical intelligence to help close care gaps

January 31, 2026January 31, 2026
Impact of Mobilization Facilitated by Wearable Device Enhanced Patient Monitoring/Electrophysiology Pod–Based Feedback on Postoperative Complications Following Colorectal Cancer Surgery: Randomized Controlled Trial

Impact of Mobilization Facilitated by Wearable Device Enhanced Patient Monitoring/Electrophysiology Pod–Based Feedback on Postoperative Complications Following Colorectal Cancer Surgery: Randomized Controlled Trial

January 31, 2026January 31, 2026
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Tag: FDA 510(k) clearance

AccurKardia Secures Second FDA Clearance for AccurECG 2.0 to Tackle Cardiac Backlogs

AccurKardia Secures Second FDA Clearance for AccurECG 2.0 to Tackle Cardiac Backlogs

January 9, 2026January 10, 2026HIT Consultant

What You Should Know

– AccurKardia has announced its second FDA 510(k) clearance for the AccurECG™ Analysis System (v2.0). This enterprise-grade, cloud-based platform is designed to ingest data from any ECG hardware—including patches and Holters—and…

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FDA Clears Ceribell’s AI-Powered EEG as First Device for Continuous Delirium Monitoring

FDA Clears Ceribell’s AI-Powered EEG as First Device for Continuous Delirium Monitoring

December 12, 2025December 13, 2025HIT Consultant

What You Should Know: 

– Ceribell, Inc. has secured FDA 510(k) clearance for the world’s first continuous, AI-powered delirium monitoring solution, expanding its existing EEG platform beyond seizure detection. 

– The technology addresses a massive gap…

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Peerbridge Health Raises $7M, Appoints MedTech Veteran Dan Reuvers to Board

Peerbridge Health Raises $7M, Appoints MedTech Veteran Dan Reuvers to Board

September 16, 2025September 17, 2025HIT Consultant

What You Should Know: 

– Peerbridge Health, a company transforming how heart disease is diagnosed has closed its latest fundraising round, raising $7M to support the commercial rollout of its new product. 

– Additionally, it has…

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GE HealthCare Launches AI-Powered Cardiovascular Ultrasound System

GE HealthCare Launches AI-Powered Cardiovascular Ultrasound System

August 29, 2025August 30, 2025HIT Consultant

What You Should Know:

– GE HealthCare announced the launch of the Vivid™ Pioneer, an advanced and adaptive cardiovascular ultrasound system. The system, which recently received CE Mark and U.S. FDA 510(k) clearance, is designed…

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DeepHealth Receives FDA Clearance for Remote Scanning Solution, TechLive™

DeepHealth Receives FDA Clearance for Remote Scanning Solution, TechLive™

August 7, 2025August 8, 2025HIT Consultant

What You Should Know: 

– DeepHealth, a subsidiary of RadNet, has received FDA 510(k) clearance for its new remote scanning solution, TechLive™. The vendor-agnostic platform is designed to address the growing radiology technologist shortage by…

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Mendaera gets FDA 510(k) clearance for handheld robotic system

Mendaera gets FDA 510(k) clearance for handheld robotic system

July 9, 2025July 9, 2025MobiHealthNews

Mendaera, a robotics company, announced it has been granted FDA 510(k) clearance for Focalist, a handheld robotic system, which aims to combine handheld robotics with real-time imaging to enable clinicians to place needles with…

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Aktiia gets FDA clearance for OTC cuffless blood pressure monitor

Aktiia gets FDA clearance for OTC cuffless blood pressure monitor

July 7, 2025July 7, 2025MobiHealthNews

Healthcare technology company Aktiia has received FDA 510(k) clearance for its over-the-counter cuffless blood pressure monitor, G0 Blood Pressure Monitoring System, also known as the Hilo Band. Aktiia’s blood pressure system, known under the Hilo…

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Fasikl's NeuroAI Wristband for essential tremor gains FDA clearance

Fasikl’s NeuroAI Wristband for essential tremor gains FDA clearance

July 3, 2025July 4, 2025MobiHealthNews

Minneapolis-based Fasikl has received FDA 510(k) clearance for its Felix NeuroAI Wristband for adults with essential tremor. The wearable combines AI and neurotechnology to modulate the nervous system to help alleviate functional limitations caused by…

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HealthpointCapital acquires surgical extended reality company

HealthpointCapital acquires surgical extended reality company

July 1, 2025July 1, 2025MobiHealthNews

Private equity firm HealthpointCapital, which focuses on the musculoskeletal care sector, has acquired a majority stake in ImmersiveTouch, a medical extended reality (medical XR) company that enables surgeons to visualize and plan surgeries. Extended reality…

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Atraverse Medical secures $29.4M in financing for expansion

Atraverse Medical secures $29.4M in financing for expansion

June 11, 2025June 11, 2025MobiHealthNews

Atraverse Medical, a medical device company involved in minimally invasive cardiac procedures, announced the close of a $29.4 million follow-on financing.The raise expands upon $12.5 million in prior seed investment, which was utilized to…

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The most evolutionary change coming to hospital rooms of the future is that they will be in your own home. For certain acute conditions, the hospital room will come to you. You will be able to convalesce in the comfort of your own home by using portable technology and next-generation healthcare equipment. This will allow for high quality care to be rendered in a person's home by medical professionals both onsite and virtually.

Nick Patel

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