Press Releases April 8, 2026 08:00 AM

Catheter Precision to Attend the Annual European Heart Rhythm Association Conference

Catheter Precision to Showcase Advanced Cardiac Devices at European Heart Rhythm Association Conference

By Caleb Monroe VTAK
Catheter Precision to Attend the Annual European Heart Rhythm Association Conference
VTAK

Catheter Precision, Inc. announced its participation in the European Heart Rhythm Association conference in Paris, highlighting its LockeT suture retention device which recently received CE Mark approval and its VIVO 3D imaging system. The company's presence at EHRA aims to educate physicians and distributors to expand the use of its innovative electrophysiology products in cardiovascular care.

Key Points

  • Catheter Precision will attend EHRA 2026 in Paris to present its cardiac electrophysiology technologies, including LockeT and VIVO.
  • LockeT, a suture retention device for wound closure, has obtained CE Mark approval and is FDA registered, enabling wider European market access.
  • VIVO, a non-invasive 3D imaging system for ventricular arrhythmias, holds marketing clearance from the U.S. FDA and CE Mark, supporting its adoption in clinical practice.
  • The company's participation signifies strategic efforts to connect with key opinion leaders and expand product adoption in the electrophysiology and cardiovascular device sectors.

FORT MILL, S.C., April 08, 2026 (GLOBE NEWSWIRE) -- Catheter Precision, Inc. (NYSE American: VTAK) (“VTAK” or the “Company”) today announced that it will be attending the annual European Heart Rhythm Association (EHRA) conference in Paris, France from April 12-14, 2026.

EHRA is one of several conferences supported by the European Society of Cardiology whose mission is to reduce the number of people with cardiovascular diseases by connecting cardiovascular health professionals around the world to disseminate the latest knowledge, innovations and guidelines. As a community, they work together to empower healthcare providers to transform cardiovascular care from a privilege to a universal right.

David Jenkins, CEO of Catheter Precision, says, “Conferences continue to be a top priority for Catheter Precision. It is at these events that we can share our newest data and meet with key opinion leaders in the electrophysiology field. EHRA 2026 is exciting as this is the first large European conference we are attending since receipt of the CE Mark for LockeT. This is the perfect opportunity to educate new physicians and distributors about LockeT and continue the forward momentum and expanded product use.”

About LockeT
Catheter Precision’s LockeT is a suture retention device intended to assist in wound closure after percutaneous venous punctures. LockeT is a Class 1 device registered with the FDA and has received CE Mark approval.

About VIVO™
Catheter Precision’s VIVO (View Into Ventricular Onset), is a non-invasive 3D imaging system that enables physicians to identify the origin of ventricular arrhythmias pre-procedure, thereby streamlining workflow and reducing procedure time. VIVO has received marketing clearance from the U.S. FDA and has the CE Mark.

About Catheter Precision
Catheter Precision is an innovative U.S.-based medical device company bringing new solutions to market to improve the treatment of cardiac arrhythmias. It is focused on developing groundbreaking technology for electrophysiology procedures by collaborating with physicians and continuously advancing its products.

Cautionary Note Regarding Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Words such as “believe,” “expect,” “anticipate,” “potential,” “will,” “may,” and similar expressions are intended to identify forward-looking statements. These statements include, but are not limited to, expectations regarding potential strategic transactions, valuation outcomes, market opportunities, and the Company’s growth strategy. These statements involve risks and uncertainties that could cause actual results to differ materially. For a discussion of these risks, please refer to the Company’s filings with the SEC, including its most recent Forms 10-K and 10-Q. The Company undertakes no obligation to update any forward-looking statements.

CONTACTS:

Investor Relations
973-691-2000
[email protected]

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Risks

  • Forward-looking statements indicate potential uncertainties around market adoption and acceptance of new devices like LockeT and VIVO, which could impact growth.
  • Regulatory risks persist despite CE Mark and FDA clearance, including possible future compliance or approval challenges that may affect market expansion.
  • Competition in the cardiac electrophysiology device market could impact Catheter Precision's market share and revenue growth projections.

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