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CVRx to Participate at the Piper Sandler 37th Annual Healthcare Conference

Key Takeaway: CVRx, Inc. announced its participation in the Piper Sandler 37th Annual Healthcare Conference, scheduled for December 3, 2025. The management team will engage in a fireside chat that will be available via webcast. The company focuses on developing neuromodulation solutions for cardiovascular diseases, including its FDA-approved Barostim device, which addresses heart failure symptoms.

Market Sentiment Analysis

POSITIVE FACTORS

  • Participation at a reputable healthcare conference enhances visibility.
  • Focus on innovative neuromodulation solutions aligns with industry advancements.
  • FDA approval and Breakthrough Device designation for Barostim indicate regulatory support.

Full Press Release Details

MINNEAPOLIS, Nov. 19, 2025 (GLOBE NEWSWIRE) -- CVRx, Inc. (NASDAQ: CVRX) ("CVRx"), a commercial-stage medical device company focused on developing, manufacturing and commercializing innovative neuromodulation solutions for patients with cardiovascular diseases, today announced that the management team will participate in a fireside chat at the Piper Sandler 37th Annual Healthcare Conference on Wednesday, Dec. 3, 2025. The fireside chat is scheduled at 2:00 p.m. (ET) the same day via webcast.
A live audio webcast of the fireside chat will be available online at the investor relations page of the Company’s website at ir.cvrx.com.
CVRx is a commercial-stage medical device company focused on developing, manufacturing and commercializing innovative neuromodulation solutions for patients with cardiovascular diseases. Barostim™ is the first medical technology approved by FDA that uses neuromodulation to improve the symptoms of patients with heart failure. Barostim is an implantable device that delivers electrical pulses to baroreceptors located in the wall of the carotid artery. The therapy is designed to restore balance to the autonomic nervous system and thereby reduce the symptoms of heart failure. Barostim received the FDA Breakthrough Device designation and is FDA-approved for use in heart failure patients in the U.S. It has been certified as compliant with the EU Medical Device Regulation (MDR) and holds CE Mark approval for heart failure and resistant hypertension in the European Economic Area. To learn more about Barostim, visit www.cvrx.com.
Mark Klausner or Mike Vallie

Frequently Asked Questions

What is the CVRx company known for?

CVRx focuses on innovative neuromodulation solutions for cardiovascular diseases.

When is the Piper Sandler Healthcare Conference for CVRx?

The CVRx fireside chat at the conference is on December 3, 2025, at 2:00 p.m. ET.

What is Barostim designed to treat?

Barostim is intended to alleviate symptoms of heart failure.

Is Barostim FDA approved?

Yes, Barostim is FDA-approved for use in heart failure patients.

Where can I access the fireside chat webcast?

The webcast will be available on the CVRx investor relations page online.

Last updated: Nov 19, 2025