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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: Food and Drug Administration

Welldoc Awarded FDA 510(k) Clearance for Diabetes Platform

Welldoc Awarded FDA 510(k) Clearance for Diabetes Platform

August 23, 2023August 24, 2023HIT Consultant

What You Should Know:

Welldoc®, a digital health leader revolutionizing chronic care, today announced the receipt of its 11th 510(k) clearance from the Food and Drug Administration (FDA) for its award-winning diabetes digital health solution,…

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Proprio Raises $43M Series B Funding to Fuel Commercialization | Healthcare IT Today

Proprio Raises $43M Series B Funding to Fuel Commercialization | Healthcare IT Today

August 17, 2023August 17, 2023Healthcare IT Today

First Light Field-Enabled Surgical Technology Company Secures Additional Institutional Capital to Drive Adoption of its AI-Driven Platform
Proprio, a Seattle-based surgical technology company, today announced that it has secured $43 million in Series B funding…

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Viz.ai gets FDA De Novo approval for AI-enabled heart disease detection

Viz.ai gets FDA De Novo approval for AI-enabled heart disease detection

August 17, 2023August 17, 2023Healthcare IT news

The U.S. Food and Drug Administration’s approval of Viz.ai’s hypertrophic cardiomyopathy establishes a new category for cardiovascular machine learning-based notification software.WHY IT MATTERS
Viz.ai, a disease detection and intelligent care coordination company, said in its…

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FemTech: First Women’s Medical-Grade Wearable Smart Ring Submitted for FDA Clearance

FemTech: First Women’s Medical-Grade Wearable Smart Ring Submitted for FDA Clearance

August 3, 2023August 4, 2023HIT Consultant

What You Should Know:  Movano Health, makers of the Evie Ring, the first medical-grade wearable smart ring for women announced that it has submitted a 510(k) premarket notification to the U.S. Food and Drug…

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4 ways biopharma is applying AI/ML to improve drug development outcomes - MedCity News

4 ways biopharma is applying AI/ML to improve drug development outcomes – MedCity News

July 31, 2023August 1, 2023MedCity News

Healthcare innovation in drug development intersects with a few critical trends: the rise of artificial intelligence (AI) applications in healthcare—particularly machine learning (ML) and predictive analytics; the need to reduce the costs associated with…

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Roundup: Nesa gets US FDA 510(k) for fibroid mapping tool and more briefs

Roundup: Nesa gets US FDA 510(k) for fibroid mapping tool and more briefs

July 29, 2023July 30, 2023MobiHealthNews

Nesa obtains US FDA 510(k) for fibroid mapping techIndian femtech Nesa Medtech has received the United States Food and Drug Administration 510(k) clearance for its fibroid mapping tool.
Its Fibroid Mapping Reviewer Application assists in…

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MedCrypt, Kansas State University Launch Medical Device Security Research Project

MedCrypt, Kansas State University Launch Medical Device Security Research Project

July 12, 2023July 13, 2023Health IT Security

By Jill McKeon

July 12, 2023 – MedCrypt, a cybersecurity solution provider for medical device manufacturers, announced a partnership with Kansas State University (KSU) to drive medical device security research. MedCrypt provided a grant to KSU…

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Roundup: South Korean AI software for sepsis detection gets US FDA nod and more briefs

Roundup: South Korean AI software for sepsis detection gets US FDA nod and more briefs

June 23, 2023June 24, 2023MobiHealthNews

SpassMed scores US FDA 510(k) for AI sepsis detection softwareSouth Korean medical AI company SpassMed has received the United States Food and Drug Administration’s 510(k) clearance for its AI-powered sepsis detection software. 
The AI solution…

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New FDA Draft Guidance Signals Acceptance of Decentralized Trials (When Done Right) - MedCity News

New FDA Draft Guidance Signals Acceptance of Decentralized Trials (When Done Right) – MedCity News

June 13, 2023June 13, 2023MedCity News

When regulators speak, we listen.
Naturally risk-averse industries like the life sciences need health authority acceptance before trying new approaches and especially before committing to wholesale operational change, even if the outcome has great potential….

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GE Healthcare's DL model for cardiac MRI gains FDA clearance

GE Healthcare’s DL model for cardiac MRI gains FDA clearance

June 12, 2023June 13, 2023Healthcare IT news

GE Healthcare announced that the U.S. Food and Drug Administration has cleared Sonic DL, which leverages a neural network to accelerate image acquisition in magnetic resonance imaging, for healthcare use. WHY IT MATTERS
The need for…

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You have to understand what are they worried about, what are their fears, what are they trying to do? If we don’t engage with them that way, it doesn’t matter what technology we use.

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