Press Releases April 27, 2026 04:30 PM

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

CVRx Announces Q1 2026 Earnings Release and Conference Call Date

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

CVRx, a medical device company specializing in neuromodulation therapies for cardiovascular diseases, announced it will report its first quarter 2026 financial and operating results after market close on May 11, 2026, followed by a conference call. The company focuses on its FDA-approved Barostim therapy for heart failure patients.

Key Points

  • CVRx is a commercial-stage medical device company with the FDA-approved Barostim neuromodulation therapy targeting heart failure.
  • The company plans to release Q1 2026 results and host a conference call on May 11, 2026.
  • Barostim holds FDA Breakthrough Device designation and CE Mark certification for use in the U.S. and European markets.

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 at ir.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 Vallie
ICR Healthcare
443-213-0501
[email protected]

Media Contact:
Emily Meyers
CVRx, Inc.
763-416-2853
[email protected]


Risks

  • Financial performance may not meet market expectations leading to unfavorable investor sentiment.
  • Regulatory risks related to maintaining approvals and compliances in the U.S. and Europe.
  • Market adoption and competition within the cardiovascular medical device sector could impact commercial success.

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