News | Computed Tomography (CT) | May 19, 2025

Arineta’s Cardiac CT Scanner Receives FDA Clearance

The 510(k) clearance expands the scanner’s imaging capabilities to support early detection and diagnosis of lung cancer and associated cardiovascular conditions.

Arineta’s Cardiac CT Scanner Receives FDA Clearance

May 19, 2025 - Arineta, a provider of cardiovascular imaging solutions, recently announced that its SpotLight Duo cardiac CT scanner has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for low-dose lung cancer screening (LDCT). This clearance allows providers to use a single ultra-fast CT platform for both cardiac and lung imaging and diagnostics, delivering more complete care to high-risk patients.

Lung cancer is the leading cause of cancer deaths in the U.S., with a new patient diagnosed nearly every two minutes. However, today, more people are surviving lung cancer than ever before, and over the past five years, the survival rate has increased by 26% nationally to 28.4%. Arineta’s FDA clearance expands access to the critical, lifesaving imaging needed for this high-risk population. 

“This clearance marks a significant milestone in expanding our role in early detection and preventative care,” said Doug Ryan, CEO of Arineta. “We are dedicated to growing cardio-thoracic CT as the front-line non-invasive test for diagnosing, therapy planning, and monitoring of cardiovascular and thoracic disease. The addition of FDA clearance for Low Dose Lung Cancer CT strengthens our ability to support improved outcomes for patients at high risk of disease.”

As awareness grows around preventative imaging and population health strategies, this clearance expands the clinical utility of Arineta’s SpotLight Duo across health systems, provider offices, mobile scanning units, and imaging centers nationwide. With the addition of this clinical application for LDCT, the system supports earlier detection and more proactive care for patients.

The Spotlight Duo cardiac CT scanner captures the entire heart in a single beat, featuring 140 mm coverage at a rotation speed of 0.24 sec per rotation. Its advanced deep-learning imaging reconstruction (DLIR) technology enhances image quality by reconstructing cross-sectional images, resulting in more comprehensive and accurate diagnoses.

For more information, visit arineta.com


Related Content

News | FDA

Jan. 13, 2026 – Innovative Health, Inc. has received its 50th clearance from FDA to reprocess single-use medical devices ...

Home January 15, 2026
Home
News | FDA

Jan. 12, 2026 — HeartLung Corp. has announced U.S. Food and Drug Administration (FDA) clearance of AI-CVD, its AI ...

Home January 12, 2026
Home
News | FDA

Jan. 6, 2026 — W. L. Gore & Associates’ medical business (Gore) has announced the FDA approval of the Gore Viabahn ...

Home January 06, 2026
Home
News | FDA

Dec. 22, 2025 — Abbott recently announced the U.S. Food and Drug Administration (FDA) has approved the company's Volt ...

Home January 05, 2026
Home
News | FDA

Dec. 18, 2025 — Huxley Medical has announced the SANSA home sleep apnea test has received regulatory clearance from the ...

Home December 19, 2025
Home
News | FDA

Dec. 18, 2025 — Abbott has received U.S. Food and Drug Administration (FDA) clearance and CE Mark for its Amplatzer ...

Home December 18, 2025
Home
News | FDA

Dec. 15, 2025 — HeartSciences Inc., a healthcare information technology company advancing the use of ECG/EKGs through ...

Home December 16, 2025
Home
News | FDA

Nov. 25, 2025 — Remington Medical has received U.S. Food and Drug Administration (FDA) 510(k) clearance and announced ...

Home December 09, 2025
Home
News | FDA

Dec. 3, 2025 — Atraverse Medical, a medical device company developing next-generation left-heart access technology, has ...

Home December 05, 2025
Home
News | FDA

Dec.1, 2025 – MannKind Corp. has announced that the U.S. Food and Drug Administration (FDA) has accepted the sNDA ...

Home December 01, 2025
Home
Subscribe Now