Press Releases May 20, 2026 04:30 PM

CVRx to Present at the William Blair 46th Annual Growth Stock Conference

CVRx Announces Upcoming Presentation at William Blair Growth Stock Conference

By Jordan Park CVRX

CVRx, Inc., a commercial-stage medical device company specializing in neuromodulation solutions for cardiovascular diseases, announced that its management team will present at the William Blair 46th Annual Growth Stock Conference on June 2, 2026. The company highlighted its FDA-approved Barostim device aimed at treating heart failure through neuromodulation technology.

CVRx to Present at the William Blair 46th Annual Growth Stock Conference
CVRX

Key Points

  • CVRx focuses on innovative neuromodulation devices for cardiovascular disease treatment.
  • Barostim, CVRx's lead product, is FDA-approved for heart failure and holds CE Mark for European markets.
  • The company will present its growth and product advancements at a prominent investor conference, enhancing visibility with investors in healthcare and medical technology sectors.

MINNEAPOLIS, May 20, 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 William Blair 46th Annual Growth Stock Conference in Chicago on Tuesday, June 2, 2026. The Company's presentation will begin at 10:40 a.m. (CT).

A live webcast of the event can be found at ir.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 An archived version of the presentation will be available following the live event and can be accessed at the same location for a limited time.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.

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

  • Market adoption and reimbursement challenges for Barostim could impact commercial success.
  • Regulatory environment changes in the U.S. and Europe might affect product approvals and sales.
  • Competitive pressure in the medical device and cardiovascular treatment sectors could limit market share growth.

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