Welcome to our dedicated page for Catheter Precision news (Ticker: VTAK), a resource for investors and traders seeking the latest updates and insights on Catheter Precision stock.
Catheter Precision Inc. (VTAK) delivers innovative electrophysiology solutions through its VIVO cardiac mapping system and LockeT vascular closure technology. This page serves as the definitive source for official company announcements, clinical trial updates, and strategic developments in non-invasive cardiac care.
Investors and medical professionals will find curated press releases covering regulatory milestones, product innovations, and partnership agreements. Our repository includes updates on FDA clearances, international distribution expansions, and peer-reviewed study results validating device efficacy.
Key content categories include quarterly financial results, technology enhancements to the VIVO 3D imaging platform, and clinical outcomes data for the suture retention system. All materials maintain compliance with financial disclosure regulations while emphasizing patient-centered innovation in arrhythmia treatment.
Bookmark this page for real-time updates on Catheter Precision's advancements in electrophysiology and vascular closure solutions. Visit regularly to stay informed about developments impacting cardiac care technology and investment considerations.
Catheter Precision (NYSE American: VTAK) has received CE Mark approval for LockeT, its advanced vascular closure device, enabling market access in the EU, UK, Switzerland, and Turkey. The European Vascular Closure Devices Market, valued at $3.1 billion in 2024, is projected to reach $4.3 billion by 2028 with a 7% CAGR.
The company has already secured its first order of 100 units and is in discussions with multiple distribution partners. LockeT offers economic advantages over competing products and features easy deployment, patient comfort, and intuitive recovery nursing processes.
Catheter Precision (VTAK) has secured a $1.5 million private placement equity financing and acquired promissory notes of QHSLab. The financing involves selling 1,500 shares of Series B Preferred Stock convertible into 4,287,000 common shares, along with 4,285,716 warrants at a $0.50 exercise price. Additionally, the company issued another 1,500 preferred shares to acquire QHSLab's senior secured notes worth approximately $1.6 million.
The strategic move aims to expand Catheter Precision's reach into general cardiology and cardiac electrophysiology with office-oriented product lines. QHSLab operates in physician marketplaces, offering diagnostic solutions for mental health, cardiology, drug compliance, and allergy analyses. Ladenburg Thalmann & Co. served as the exclusive placement agent for these transactions.
Catheter Precision (VTAK) announced its participation in the 46th annual Heart Rhythm Society (HRS) meeting from April 24-27, 2025, in San Diego. The conference will gather nearly 10,000 professionals in arrhythmia care and electrophysiology, featuring over 200 educational sessions and 3,400 scientific abstracts.
The company will present four research abstracts at HRS 2025: three for VIVO and one for LockeT. Key findings include:
- VIVO showed 94% accuracy in a 125 multi-center European study with 83% long-term procedural success
- Research demonstrating VIVO's effectiveness in mapping difficult-to-identify PVCs
- LockeT's safety and efficacy study in 139 patients for large-bore access procedures
- VIVO's 89% accuracy in predicting exit site locations for scar-dependent VT, with 86% of patients free from device therapy after one year
Catheter Precision (VTAK) has signed a definitive agreement to acquire assets related to the Cardiac Pulmonary Nerve Stimulation (CPNS) System through its 82% owned subsidiary, Cardionomix. The CPNS System, developed by Cardionomic, targets acute decompensated heart failure (ADHF) treatment through electrical stimulation via a temporary catheter.
The acquisition terms include 1,000,000 unregistered common stock shares and a $1.5 million three-year promissory note at 4% annual interest through Cardionomix. Initial clinical studies showed promising results, including reduced heart failure worsening, increased fluid loss, improved quality of life, and reduced mortality.
The technology addresses a market of approximately 1 million annual U.S. hospital admissions for heart failure, with potential annual revenues exceeding $1 billion. The Cleveland Clinic Foundation, Abbott Laboratories, and New Era Associates will receive economic interests in VTAK common stock and Cardionomix note as current creditors.