Recent Updates
Recently added Catalysts
CVRX Positive Sentiment Score: 70/100

CVRx to Report First Quarter 2025 Financial and Operating Results and Host Conference Call on May 8, 2025

Key Takeaway: CVRx, Inc. (NASDAQ: CVRX) has announced that it will report its first quarter 2025 financial and operating results after the market closes on May 8, 2025. Following the announcement, the company will host a conference call to discuss these results at 4:30 PM Eastern Time. CVRx specializes in developing neuromodulation solutions for cardiovascular diseases, with its Barostim device being the first FDA-approved technology of its kind for heart failure patients.

Market Sentiment Analysis

POSITIVE FACTORS

  • CVRx is set to release its first quarter 2025 financial results, indicating ongoing operational activity.
  • The Barostim device is FDA-approved and recognized as a Breakthrough Device, highlighting its innovative approach.
  • CVRx's focus on neuromodulation solutions addresses significant health issues in cardiovascular diseases.

Full Press Release Details

MINNEAPOLIS, April 24, 2025 (GLOBE NEWSWIRE) -- CVRx, Inc. (NASDAQ: CVRX) ("CVRx"), a commercial-stage medical device company, today announced that it plans to release first quarter 2025 financial and operating results after market close on Thursday, May 8, 2025. The Company will host a conference call to review its results at 4:30pm Eastern Time the same day.
A live webcast of the investor conference call will be available online at the investor relations page of the Company’s website at ir.cvrx.com. To listen to the conference call on your telephone, please dial 1-800-445-7795 for U.S. callers, or 1-785-424-1699 for international callers, approximately ten minutes prior to the start time. Please reference the following conference ID to access the call: CVRXQ125.
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 also received the CE Mark 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

When will CVRx announce its Q1 2025 financial results?

CVRx will announce Q1 2025 results on May 8, 2025, after market close.

How can I listen to the CVRx conference call?

You can listen by dialing 1-800-445-7795 for U.S. callers or 1-785-424-1699 internationally.

What is Barostim used for?

Barostim is an implantable device that treats heart failure symptoms using neuromodulation.

Is Barostim FDA-approved?

Yes, Barostim is FDA-approved for heart failure and received Breakthrough Device designation.

Where can I find more information about Barostim?

More information about Barostim is available on CVRx's website at www.cvrx.com.

Last updated: Apr 24, 2025