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Hyperfine Announces FDA Clearance of Software Update That Enables Faster Acquisition of Best-in-Class Ultra-Low-Field Brain Images

Imaging Technology

mtaschetta-millane Wed, 07/17/2024 - 10:52 July 17, 2024 — Hyperfine , a groundbreaking medical device company that has redefined brain imaging with the world’s first FDA-cleared portable magnetic resonance brain imaging system—the Swoop system—announced the clearance of the ninth generation of AI-powered Swoop system software.

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InkSpace Imaging receives FDA Clearance for a 24-channel Small Body Array Compatible with Siemens Healthineers 3T Systems

Imaging Technology

milla1cf Fri, 01/26/2024 - 21:11 January 26, 2024 — InkSpace Imaging , a leader in innovative diagnostic medical device technology, is proud to announce it received FDA clearance for its next-generation Small Body Array for the Siemens Healthineers Magnetom Skyra and Vida series 3T MRI scanners.

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Hyperfine, Inc. Receives FDA Clearance for Updated AI-powered Software with Improved Image Quality for All Swoop System Sequences

Imaging Technology

a groundbreaking medical device company that has redefined brain imaging with the world’s first FDA -cleared portable magnetic resonance brain imaging system—the Swoop system—announced FDA clearance of updated software. We believe in making brain imaging more accessible, clinically relevant, and actionable. “We

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ACR responds to Congressional query on AI reimbursement

AuntMinnie

MD, issued a nine-page letter to Congress recommending how to solve the reimbursement problem for AI in healthcare and ensure clinical AI is of value to patients and health systems. Proactive facility cybersecurity for protecting sensitive patient data that serves as the input or output of the AI. William Thorwarth Jr.,

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Positron Corporation Joins Cardiac PET Industry Coalition (CPIC)

Imaging Technology

Positron joins forces with the coalitions founding members, Bracco Diagnostics , CDL Nuclear Technologies and Siemens Healthcare who have come together to promote federal policies that advance health outcomes for patients with cardiovascular disease and improve the availability of cardiac PET diagnostics throughout the United States.

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XEOS Receives Approval by US FDA for the AURA 10 PET-CT Specimen Imager for the Operating Room

Imaging Technology

milla1cf Thu, 09/07/2023 - 13:59 September 7, 2023 — The groundbreaking AURA 10 specimen imager by Belgian MedTech pioneer XEOS has been cleared by the FDA. This advancement promises to transform the landscape of intraoperative diagnostics, offering real-time insights that can make all the difference in patient care.

Imaging 105
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Pixyl receives FDA clearance for AI-powered brain MRI software Pixyl.Neuro

Imaging Technology

Pixyl is an award-winning French medtech specializing in AI-powered MRI solutions to improve patient care. AI-driven MRI analysis opens the possibility of accessing previously unavailable clinically-relevant information to reinforce radiology workflows, especially in the context of neurological disorders.” explains Pr.

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