GE HealthCare expands the LOGIQ e ultrasound platform with new LOGIQ e family

Key Terms

510(k) regulatory

A 510(k) is a U.S. regulatory submission that a medical device maker uses to show a new device is as safe and effective as an already-approved device, allowing the regulator to clear it for sale rather than requiring the longer, more stringent approval process. For investors, a cleared 510(k) usually means lower regulatory risk and a faster path to market, which can speed revenue generation and reduce uncertainty—similar to proving a new appliance works like a trusted existing model.

ce mark regulatory

A CE mark is a regulatory stamp placed on products to show they meet the European Union’s basic safety, health and environmental rules and can be sold in the European Economic Area. For investors it matters because the mark unlocks market access, affects how quickly a product can generate revenue, and signals regulatory risk and potential compliance costs—think of it as a passport that lets a product enter a large market.

left ventricle medical

The left ventricle is one of the heart’s four chambers, responsible for pumping oxygen-rich blood from the heart into the body through the main artery. It matters to investors because left ventricle function is a key measure in clinical trials, medical device performance, and drug safety; think of it as the engine cylinder whose strength and efficiency determine overall heart output, so changes in its function can affect healthcare revenues and regulatory outcomes.

biometry medical

Measurement and analysis of biological characteristics or signals—such as fingerprints, facial features, iris patterns, heart rhythms, or medical measurements like organ size—used for identification, diagnosis, or tracking health. It matters to investors because biometry underpins products, regulatory filings, and data-privacy risks in healthcare and security markets; reliable biometric measurements can determine a device’s performance, marketability, and compliance, much like a ruler and scale determine whether a product meets a specification.

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• LOGIQ™ e Xⁱ and LOGIQ™ e Sⁱ offer console-quality ultrasound in a compact laptop-sized system anywhere care can be deliveredⁱⁱ

CHICAGO--(BUSINESS WIRE)-- GE HealthCare today announced the introduction of the LOGIQ™ e family, featuring LOGIQ™ e Xⁱ and LOGIQ™ e Sⁱ, two compact laptop ultrasound systems designed to help clinicians deliver simple, fast, and confident ultrasound imaging where it’s needed across care settings.ⁱⁱ Building on the legacy of LOGIQ e, the LOGIQ e family pairs a reliable console-level performance with a compact, intuitive design combining AI-powered featuresⁱⁱⁱ and workflow tools that support portability and flexibility for care beyond traditional imaging departments.

“Healthcare delivery is changing rapidly, and imaging technology must evolve with it. Clinicians today need imaging solutions that can move seamlessly across care settings while supporting a variety of users and clinical applications,” said Karley Yoder, CEO, Ultrasound Solutions, Advanced Imaging Solutions, GE HealthCare. “The LOGIQ e family furthers our ability to serve customers with solutions that balance portability, performance and workflow, while bringing the right imaging capabilities to the right clinical environments.”

The LOGIQ e family supports a broad range of clinical applications including multi-purpose imaging, musculoskeletal, emergency medicine, critical care, rheumatology and anesthesiology. LOGIQ e Xⁱ is a premium offering that combines AI-powered tools, advanced imaging capabilities and workflow-enhancing features, while LOGIQ e Sⁱ provides essential imaging capabilities in an intuitive, reliable system at a more affordable price point. Together, the systems give clinicians new options built to support a range of user preferences and operational requirements.

To help clinicians keep pace in busy environments, the LOGIQ e family features workflow tools like Scan Assistantⁱⁱⁱ and Voice Control, to help reduce manual interactions and increase efficiency. Depending on configuration and region, LOGIQ e Xⁱ also includes AI-powered tools designed to assist clinicians with image acquisition and workflow efficiency during exams:

• Nerveblox™^iv labels anatomical landmarks in the ultrasound image, designed to help clinicians feel confident during the peripheral nerve block procedure.
• MSK Go^v assists clinicians in performing musculoskeletal ultrasound examinations, identifying anatomical structures on the ultrasound images acquired.

The ultrasound system also offers new tools to help enhance clinician confidence:

• B-Flow provides real-time, high-resolution imaging of blood flow.
• Speckle Reduction Imaging (SRI)-HD enhances visibility of organs and lesions with high-definition contrast resolution.
• Automated Function Imaging (AFI)ⁱⁱⁱ assesses structural heart defects of the left ventricle, right ventricle and left atrium throughout the heart cycle.
• SonoBiometry performs measurements of fetal head, abdomen and femur, reducing keystrokes and improving workflow efficiency in biometry exams.

Verisound™ digital tools are also available depending on product configuration and region. Verisound Fleet, a cloud-based fleet management solution, supports organizations managing multiple systems with remote system configuration and backup, fleet-wide deployment capabilities. Verisound Collab^vi enables virtual collaboration, and real-time system usage collaboration that lets clinicians easily communicate and collaborate within their network. LOGIQ e Xⁱ also supports Vscan Air™ probe compatibility, giving clinicians added flexibility with wireless, cable-free scanning.

“As I work in different clinics, a portable device is essential for me. What first caught my attention with the LOGIQ e is its design but beyond it being appealing is its performance, it’s very practical, easy to use and simple,” said Dr. Vicente Roqués Escolor, anesthesiologist. “I was also impressed by the possibility of using artificial intelligence, specifically the Nerveblox tool, which allows the scouting of the different structures we see in a large number of regional anesthesia techniques before performing the intervention.”

The latest LOGIQ e ultrasound systems are 510(k) cleared and CE Marked. These ultrasound systems are available in other markets where regulatory approval has been granted. For more information on LOGIQ e family, visit: https://www.gehealthcare.com/en/products/ultrasound/point-of-care-ultrasound/logiq-e-ultrasound and https://www.gehealthcare.com/en/products/ultrasound/versana/logiq-e-s.

About GE HealthCare Technologies Inc.

GE HealthCare is a leading global healthcare solutions provider of advanced medical technology, pharmaceutical diagnostics, and AI, cloud and software solutions that help clinicians tackle the world’s most complex diseases. Serving patients and providers for 130 years, GE HealthCare is delivering bold innovations designed for the next era of medicine across its Advanced Imaging Solutions, Pharmaceutical Diagnostics and Patient Care Solutions segments to help clinicians deliver more personalized, precise patient care. We are a $20.6 billion business with approximately 54,000 colleagues working to create a world where healthcare has no limits.

GE HealthCare is proud to be among 2026 Fortune World’s Most Admired Companies™.

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ⁱ LOGIQ e X and LOGIQ e S are marketing representations of the LOGIQ e product; feature availability may vary depending on region.
ⁱⁱ The device is intended for use in professional healthcare facilities. Use is restricted to environmental properties described in the user manual.
ⁱⁱⁱ Only available on LOGIQ e X.
^iv Nerveblox is a trademark of Smart Alfa Teknoloji San. ve Tic. A.S.
^v MSK Go is powered by SmartAlpha.
^vi Not for diagnostic use.

View source version on businesswire.com: https://www.businesswire.com/news/home/20260804316542/en/

GE HealthCare Media Contact:
Eric Tatro
M +1 312 459 6140
eric.tatro@gehealthcare.com

Source: GE HealthCare Technologies Inc.