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CVRx to Present at the Goldman Sachs 47th Annual Global Healthcare Conference

Key Takeaway: CVRx, Inc. will present at the Goldman Sachs 47th Annual Global Healthcare Conference on June 10, 2026. The presentation will highlight their innovative neuromodulation solutions for cardiovascular diseases, particularly the Barostim device, which is FDA-approved for heart failure. A live webcast will be available for interested parties.
Price reaction · baseline $6.08 (2026-05-26 close) · hit after-hours · clean, no other CVRX news in the window
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POSITIVE FACTORS

  • CVRx is presenting at a significant healthcare conference.
  • The company focuses on innovative solutions for cardiovascular diseases.
  • Barostim has received FDA Breakthrough Device designation.

Full Press Release Details

MINNEAPOLIS, May 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, announced today that the management team will present at the Goldman Sachs 47thAnnual Global Healthcare Conference in Miami on Wednesday, June 10, 2026. The Company's presentation will begin at 8:00 a.m. (ET).
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 An archived version of the presentation will be available following the live event and can be accessed at the same location for a limited time.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, visit www.cvrx.com.

Frequently Asked Questions

When will CVRx present at the Goldman Sachs conference?

CVRx will present on June 10, 2026, at 8:00 a.m. ET.

What is Barostim used for?

Barostim is used to improve symptoms in patients with heart failure.

Where can I watch the CVRx presentation?

A live webcast will be available at ir.cvrx.com.

What regulatory approvals does Barostim have?

Barostim is FDA-approved and holds CE Mark approval in Europe.

Last updated: May 27, 2026