Press Releases July 28, 2026 08:30 AM

CVRx to Present at Canaccord Genuity's 46th Annual Growth Conference

CVRx to Present at Canaccord Genuity's 46th Annual Growth Conference on August 11, 2026

By Derek Hwang
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CVRx, Inc., a medical device company specializing in neuromodulation solutions for cardiovascular diseases, announced that its management team will present at Canaccord Genuity's 46th Annual Growth Conference. The company highlights its FDA-approved Barostim device which addresses heart failure symptoms through neuromodulation technology.

CVRx to Present at Canaccord Genuity's 46th Annual Growth Conference
CVRX
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Key Points

  • CVRx management will present at a notable investor conference, increasing company visibility.
  • Barostim is the first FDA-approved neuromodulation device for heart failure, representing innovation in cardiovascular treatment.
  • The device holds regulatory approvals including FDA Breakthrough Device designation and CE Mark, supporting its commercial adoption in the U.S. and Europe.

MINNEAPOLIS, July 28, 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 Canaccord Genuity's 46th Annual Growth Conference in Boston on Tuesday, August 11, 2026. The Company's presentation will begin at 1:00 p.m. (ET).

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 An archived version of the presentation will be available following the live event and can be accessed at the same location for a limited time.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 risk of Barostim may impact revenue growth if uptake is slower than expected.
  • Regulatory changes or challenges could affect product approvals or market access.
  • Competitive pressure in the cardiovascular medical device sector may affect market share and profitability.

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