Press Releases July 23, 2026 04:30 PM

CVRx to Report Second Quarter 2026 Financial and Operating Results and Host Conference Call on August 6, 2026

CVRx to announce Q2 2026 financial results and host investor call on August 6, 2026

By Priya Menon
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CVRX

CVRx, a commercial-stage medical device company specializing in neuromodulation therapies for cardiovascular diseases, will release its Q2 2026 financial and operational results on August 6, 2026, followed by a conference call to discuss performance and outlook. CVRx's flagship product, Barostim, is FDA-approved and CE-marked for heart failure and resistant hypertension treatment.

CVRx to Report Second Quarter 2026 Financial and Operating Results and Host Conference Call on August 6, 2026
CVRX
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Key Points

  • CVRx focuses on neuromodulation devices for cardiovascular disease, with Barostim as its main product.
  • Barostim is FDA-approved and has FDA Breakthrough Device designation, also CE-marked for EU markets.
  • The company will report its Q2 2026 financials and host a conference call to discuss results and company updates.

MINNEAPOLIS, July 23, 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 second quarter 2026 financial and operating results after market close on Thursday, August 6, 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
ir@cvrx.com

Media Contact:
Emily Meyers 
CVRx, Inc. 
763-416-2853
emeyers@cvrx.com


Risks

  • Financial performance could be impacted by competitive market dynamics in the medical device sector.
  • Regulatory approvals and compliance remain critical as Barostim expands in various markets.
  • Market adoption rates of neuromodulation therapies may affect revenue growth and profitability.

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