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CVRX Positive Sentiment Score: 70/100

CVRx to Report First Quarter 2026 Financial and Operating Results and Host Conference Call on May 11, 2026

Key Takeaway: CVRx, Inc. plans to release its first quarter 2026 financial and operating results on May 11, 2026, after market close. The company will host a conference call at 4:30 p.m. ET to discuss these results. CVRx is known for its Barostim device, which is FDA-approved for treating heart failure.

Market Sentiment Analysis

POSITIVE FACTORS

  • CVRx is set to report its financial results, indicating business activity.
  • The company is focused on innovative solutions for cardiovascular diseases.
  • Barostim is recognized as a breakthrough technology by the FDA.

Full Press Release Details

MINNEAPOLIS, April 27, 2026 (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 it plans to release first quarter 2026 financial and operating results after market close on Monday, May 11, 2026. The Company will host a conference call to review its results at 4:30 p.m. 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 atir.cvrx.com. To listen to the conference call on your telephone, please dial 1- 877-704-4453 for U.S. callers, or 1-201-389-0920 for international callers, approximately ten minutes prior to the start time.

About CVRx, Inc.

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 for heart failure and resistant hypertension in the European Economic Area. To learn more about Barostim, visit www.cvrx.com.
Investor Contact:Mark Klausner or Mike VallieICR Healthcare443-213-0501ir@cvrx.com
Media Contact:Emily MeyersCVRx, Inc.763-416-2853emeyers@cvrx.com

Frequently Asked Questions

When will CVRx report its Q1 2026 results?

CVRx will report its Q1 2026 financial results on May 11, 2026.

What time is the CVRx conference call?

The conference call is scheduled for 4:30 p.m. Eastern Time on May 11, 2026.

How can I access the CVRx conference call?

You can access the call via the investor relations page on CVRx's website or by phone.

What is Barostim?

Barostim is an FDA-approved device for heart failure that uses neuromodulation.

Is Barostim approved in Europe?

Yes, Barostim is certified compliant with EU regulations and holds a CE Mark.

Last updated: Apr 27, 2026