X1-FFR

by SpectraWAVE, Inc.  · Based in United States → — Shaping the Future of Coronary Care.
Cardiology Radiology

Contact for pricing
Regulatory Status Disclosed

Overview

X1-FFR by SpectraWAVE, Inc. is an AI-enabled, wire-free, and drug-free coronary physiology software designed to calculate fractional flow reserve (FFR) from a single angiogram. Operating as a software application on the HyperVue Imaging System, it integrates physiological assessment and intravascular imaging (DeepOCT+NIRS) onto a single clinical platform.

The software is intended for use by or under the supervision of cardiologists within cardiac catheterization laboratories. It is indicated for patients undergoing transluminal interventional procedures, such as percutaneous coronary intervention (PCI) planning and optimization.

X1-FFR integrates into the clinical workflow by utilizing a direct, real-time angiography feed. This design eliminates the need for invasive pressure wires, hyperemic drugs, and the workflow delays associated with network-based DICOM file transfers. Notable capabilities of the software include:

  • Single-View Analysis: Derives FFR values using only one angiographic view per vessel.
  • AI-Driven Automation: Automatically performs vessel segmentation and frame suggestion to streamline calculations.
  • Vessel Quantification: Measures coronary vessel dimensions, quantifies stenosis, and calculates pressure drops to assist in clinical decision-making.

Reviewed by Pouyan Golshani, MD — Interventional Radiologist

Key Features

  • AI-enabled, wire-free, drug-free FFR measurement
  • Single angiogram derived physiology results
  • Rapid and accurate FFR results
  • Automated vessel segmentation
  • Automated frame suggestion
  • Eliminates DICOM file management and transfer delays
  • Software add-on to HyperVue Imaging System
  • Measurement and reporting tools for coronary vessels
  • Quantifies stenosis in coronary vessels
  • Quantifies pressure drop in coronary vessels

Use Cases

  • Assessing coronary artery disease (CAD)
  • Supporting treatment decision making during diagnostic angiograms
  • PCI planning and optimization
  • Identifying appropriate lesions for revascularization
  • Quantifying stenosis in coronary vessels
  • Quantifying pressure drop in coronary vessels

What Physicians Need to Know

Coronary Artery Assessment
X1-FFR provides rapid, accurate Fractional Flow Reserve (FFR) results from a single angiogram, eliminating the need for pressure wires and hyperemic drugs. It features AI-enabled workflows for automated vessel segmentation and frame suggestion, simplifying and speeding up FFR calculations. The software includes tools for quantifying stenosis, vessel dimensions, and pressure drop in coronary vessels.
Cardiac Monitoring Integration
The system acquires physiology results from a direct, real-time angiography feed, streamlining workflow by removing network-based DICOM file management and transfer delays.
Real-Time Alert Capability
X1-FFR delivers rapid physiology results, often in less than one minute, from a single angiogram via a direct real-time angiography feed, supporting immediate decision-making in the cath lab.
Physician Tip

Leverage X1-FFR's AI-enabled automated vessel segmentation and frame suggestion to streamline FFR assessment and accelerate results in the cath lab. Utilize the wire-free and drug-free approach to reduce procedural complexity, patient discomfort, and overall procedure time. Integrate X1-FFR with the HyperVue Imaging System for a comprehensive platform that combines angiogram-derived physiology with intravascular imaging (DeepOCT+NIRS), enabling more informed PCI planning and optimization. Recognize that this technology provides accurate FFR values from a single angiogram, offering a faster and safer alternative to traditional pressure wire-based methods for assessing coronary artery disease.

X1-FFR functions as a software add-on to SpectraWAVE's HyperVue Imaging System, creating a unified platform that integrates FDA-cleared angiogram-derived physiology with intravascular imaging capabilities (DeepOCT+NIRS). The system is designed for seamless operation within the cath lab, utilizing a direct real-time angiography feed to eliminate delays associated with network-based DICOM file transfers.

Details

Category Cardiology AI, Radiology & Imaging AI
Pricing Contact for pricing
DeploymentSoftware add-on to HyperVue Imaging System, typically deployed in cardiac cath labs.
Compliance
BAA AvailableUnknown AI-estimated
HIPAA CompliantUnknown AI-estimated
FDA Status 1 AI-estimated

SpectraWAVE, Inc. received U.S. Food and Drug Administration (FDA) 510(k) clearance (K251355) for its X1-FFR on October 17, 2025. It is cleared as a software tool that uses X-ray angiographic images to simulate coronary vascular conditions, aiding clinicians in non-invasive assessment of coronary artery disease.

Integrations
EHR Not specified
Specialties Cardiology, Radiology

What the Web Says

SpectraWAVE's X1-FFR is an AI-enabled software that provides rapid, accurate Fractional Flow Reserve (FFR) results from a single angiogram, eliminating the need for wires, drugs, and network-based DICOM file transfer delays. It integrates with the HyperVue Imaging System, creating a comprehensive platform for both angiogram-derived physiology and intravascular imaging. Physicians have expressed enthusiasm for its potential to simplify workflow, reduce user variability, and improve patient safety by offering a less invasive alternative to traditional FFR measurements.

Overall: Positive

Strengths

  • Wire-free and drug-free, making it less invasive and potentially safer for patients.
  • Provides rapid FFR results, often in less than one minute.
  • Requires only a single angiogram view, simplifying the procedure and reducing workflow complexity.
  • Utilizes AI for automated vessel segmentation and frame suggestion, enhancing speed and ease of use.
  • Eliminates network-based DICOM file management and transfer delays through a direct real-time angiography feed.
  • High concordance with invasive hyperemic pressure wire measurements in clinical analysis.

Limitations

  • As a single-view method, it may be susceptible to foreshortening errors if the initial angiographic acquisition angle is suboptimal.
  • Limited specific validation details and full publication of clinical study results are awaited to scrutinize patient selection and performance in complex anatomical subsets.
  • The information available is primarily from press releases and a review article, with no independent user reviews from platforms like Reddit, G2, or Capterra specifically for X1-FFR.

Based on reviews from: SpectraWAVE (spectrawave.com), Diagnostic and Interventional Cardiology (dicardiology.com), CRTonline (crtonline.org), MDPI (mdpi.com), Lumira Ventures (lumiraventures.com), FDA.report (fda.report)

Last updated: 2026-07-19

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Press & Coverage

Business Wire
SpectraWAVE Receives 510(k) Clearance for X1u2122-FFR, an AI-enabled, Wire-Free, Drug-Free, Single Angiogram Physiology Solution
SpectraWAVE announced FDA 510(k) clearance for its X1-FFR software, an AI-enabled, wire-free, drug-free solution that provides physiology results from a single angiogram, eliminating the need for traditional pressure wires and network-based data transfer delays.
2025-10
OEM News
FDA OKs SpectraWAVE's AI-Powered Angiogram Physiology Software
SpectraWAVE received FDA 510(k) clearance for its X1-FFR single angiogram derived physiology software, which is an add-on application to its HyperVue imaging system and provides angiogram-derived physiology and intravascular imaging on one system.
2025-10
Philips Press Release
Philips agrees to acquire SpectraWAVE Inc., advancing next-generation coronary intravascular imaging and physiological assessment with AI
Philips announced an agreement to acquire SpectraWAVE Inc., integrating SpectraWAVE's HyperVue Imaging System and X1-FFR, an AI-enabled angiography-derived FFR solution, into Philips' image-guided therapy portfolio.
2025-12
Imaging Technology News
Philips Enters Agreement to Acquire SpectraWAVE | Imaging Technology News
Philips' acquisition of SpectraWAVE will incorporate X1-FFR, an AI-enabled physiology solution that calculates Fractional Flow Reserve (FFR) from a single coronary angiogram, into its image-guided therapy platform.
2025-12
ICT&health
Philips acquires imaging company SpectraWAVE - ICT&health
Philips is strengthening its cardiac care position by acquiring SpectraWAVE, bringing technologies like HyperVue and X1-FFR, an AI-supported technology that calculates the severity of narrowing from a single X-ray image, to its portfolio.
2025-12
MDPI (International Journal of Molecular Sciences)
Fractional Flow Reserve Derived from a Single Angiographic View: Fact or Fiction?
This peer-reviewed article discusses the X1-FFR software as a commercially available add-on to the HyperVueu2122 Imaging System, highlighting its use of AI algorithms for rapid FFR calculations from a single angiogram.
2026-02
Medical Device and Diagnostic Industry
Philips Grabs AI Imaging Firm SpectraWave - Medical Device and Diagnostic industry
Philips' acquisition of SpectraWave includes the X1-FFR, an angiography-derived, AI-enabled physiology solution that calculates FFR from a single coronary angiogram for non-invasive ischemia assessment.
2025-12
PHG Stock News
Philips to acquire SpectraWAVE to expand AI coronary imaging | PHG Stock News
Royal Philips announced its agreement to acquire SpectraWAVE, which will add the HyperVue Imaging System and X1-FFR, an angiography-derived, AI-enabled FFR, to Philips' coronary intravascular imaging and physiology portfolio.
2025-12

Videos

Product demos, reviews, and walkthroughs for X1-FFR.

View all on YouTube

Frequently Asked Questions

X1-FFR integrates as a software add-on to SpectraWAVE's HyperVue Imaging System, providing rapid, wire-free, and drug-free fractional flow reserve (FFR) results from a single angiogram. It streamlines the assessment of coronary artery disease by automating vessel segmentation and frame suggestion, aiding in revascularization decisions.
X1-FFR has received U.S. Food and Drug Administration (FDA) 510(k) clearance (K251355), indicating it is substantially equivalent to a legally marketed device. As a medical device, it is designed to comply with relevant patient data privacy and security regulations, although specific details on HIPAA or GDPR compliance were not explicitly detailed in the provided information.
X1-FFR offers a wire-free and drug-free approach, unlike traditional invasive FFR which requires pressure wires and often adenosine, thereby reducing procedural complexity and patient discomfort. While other angiography-derived FFR methods exist, X1-FFR distinguishes itself by requiring only a single angiogram view and integrating AI for workflow efficiency and rapid results.
The provided information does not explicitly detail the specific pricing model for X1-FFR or its current reimbursement status. However, its recent FDA clearance and acquisition by Philips suggest it will be commercially available and integrated into existing healthcare billing structures.
While X1-FFR offers high precision and efficiency, general limitations of FFR interpretation can apply, such as the need for caution in patients with microvascular dysfunction, severe aortic stenosis, or elevated right atrial pressure. The AI in X1-FFR primarily supports workflow aspects like vessel segmentation and frame suggestion, with analytical models generating the FFR values.
X1-FFR leverages AI-enabled workflows for automated vessel segmentation and frame suggestion, which are designed to simplify and accelerate the process of obtaining FFR results. The FFR values themselves are generated using analytical (non-AI) models, and the system's FDA clearance indicates a validated level of accuracy and performance.

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Suggest an Edit → | Last Verified: 2026-04-19 | First Added: 2026-04-19
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