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Catheter Precision Announces Introduction of the LockeT Product Line into Italy

Key Takeaway: Catheter Precision, Inc. (VTAK) has announced the launch of its LockeT product line in Italy following a successful evaluation and initial procedures at ASST Valle Olona Hospital. This milestone is marked by the first purchase order from distributor Precise Srl, highlighting the product's acceptance in the market. The CEO expressed optimism about rapid uptake and the product's potential benefits for healthcare settings. LockeT is designed to aid in wound closure after venous punctures and holds FDA registration and CE Mark approval.

Market Sentiment Analysis

POSITIVE FACTORS

  • Successful introduction of LockeT into the Italian market
  • First purchase order received from a long-time partner, indicating strong market interest
  • Positive feedback from physicians and clinical acceptance in Europe
  • LockeT offers cost-effective solutions for wound closure after catheter ablation

Full Press Release Details

Fort Mill, SC, Sept. 02, 2025 (GLOBE NEWSWIRE) -- – Catheter Precision, Inc. (VTAK - NYSE/American), a US based medical device company focused on developing technologically advanced products for the cardiac electrophysiology market announced the introduction of LockeT in Italy. Following the first successful procedures and clinical acceptance in France and Germany a successful product evaluation was completed in Italy.
The first procedures in Italy were performed at ASST Valle Olona Hospital, under the expert guidance of Dr. Manuela Bianchi. These initial cases further demonstrate the versatility and clinical value of LockeT across diverse healthcare settings.
After the successful evaluation Catheter Precision received the first commercial purchase order from long-time partner and distributor Precise Srl. This milestone marks the beginning of broader market access and commercial deployment of Catheter Precision’s technologies across the region.
David Jenkins, CEO of Catheter Precision, said, “We are encouraged by the rapid uptake of LockeT acceptance in Europe, the introduction of the product into a third European country so quickly after the CE Mark approval and the first purchase order. The excitement from physicians for LockeT further demonstrates the need for a product that streamlines closure after catheter ablation procedures while remaining cost-effective.”
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 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
Statements in this press release may contain “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995 that are subject to substantial risk and uncertainties. Forward-looking statements can be identified by words such as “believe,” “anticipate,” “may,” “might,” “can,” “could,” “continue,” “depends,” “expect,” “expand,” “forecast,” “intend,” “predict,” “plan,” “rely,” “should,” “will,” “may,” “seek,” or the negative of these terms and other similar expressions, although not all forward-looking statements contain these words.  These forward-looking statements include, but are not limited to, statements regarding product evaluations at the hospital, and that the purchase order indicates that the hospital and its staff see the value and benefits that LockeT can bring and expectations regarding LockeT evaluations in the coming weeks. The Company’s expectations and beliefs regarding these matters may not materialize. Actual outcomes and results may differ materially from those contemplated by these forward-looking statements as a result of uncertainties, risks and changes in circumstances, including but not limited to risks and uncertainties included under the caption “Risk Factors” in the Company’s Form 10-K filed with the SEC and available at www.sec.gov.
The forward-looking statements included in this communication are made only as of the date hereof. The Company assumes no obligation and does not intend to update these forward-looking statements, except as required by law.

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Frequently Asked Questions

What is LockeT from Catheter Precision?

LockeT is a suture retention device designed for wound closure after venous punctures.

Where was LockeT recently introduced?

LockeT has been introduced in Italy after successful evaluations in France and Germany.

Who performed the first procedures using LockeT in Italy?

Dr. Manuela Bianchi guided the first procedures at ASST Valle Olona Hospital.

What approval has LockeT received?

LockeT is a Class 1 device registered with the FDA and has CE Mark approval.

What is Catheter Precision's focus?

Catheter Precision develops innovative medical devices for treating cardiac arrhythmias.

Last updated: Sep 2, 2025