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CVRx to Present at the 44th Annual J.P. Morgan Healthcare Conference

Key Takeaway: CVRx, Inc. will present at the 44th Annual J.P. Morgan Healthcare Conference on January 14, 2026. The presentation will showcase their innovative neuromodulation solutions for cardiovascular diseases, particularly focusing on their FDA-approved device, Barostim. A live webcast will be available, with an archived version accessible later.
Price reaction · baseline $8.03 (2025-12-19 close) · hit pre-market · clean, no other CVRX news in the window
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POSITIVE FACTORS

  • CVRx will present at a prestigious healthcare conference.
  • The company focuses on innovative solutions for cardiovascular diseases.
  • Barostim is FDA-approved and has received Breakthrough Device designation.

Full Press Release Details

MINNEAPOLIS, Dec. 22, 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 present at the 44th Annual J.P. Morgan Healthcare Conference in San Francisco on Wednesday, Jan. 14, 2026. The Company's presentation will begin at 3:45 p.m. (PT).A live webcast of the event can be found atir.cvrx.com. An archived version of the presentation will be available following the live event and can be accessed at the same location for a limited time.About CVRx, Inc.CVRx is a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 approval for heart failure and resistant hypertension in the European Economic Area. To learn more about Barostim, visitwww.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 present at the J.P. Morgan Conference?

CVRx will present on January 14, 2026, at 3:45 p.m. PT.

What is Barostim?

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

Where can I watch the CVRx presentation?

A live webcast of the presentation will be available on CVRx's investor relations site.

What designation has Barostim received from the FDA?

Barostim has received the FDA Breakthrough Device designation.

Last updated: Dec 22, 2025