Press Releases July 28, 2026 04:05 PM

Pulmonx to Present at the Canaccord Genuity 46th Annual Growth Conference

Pulmonx to Present at Canaccord Genuity 46th Annual Growth Conference Highlighting Leadership in COPD Treatment

By Nina Shah
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Pulmonx Corporation, a Nasdaq-listed company and leader in minimally invasive treatments for severe lung disease, announced its participation in a fireside chat at the Canaccord Genuity 46th Annual Growth Conference. The company will discuss its innovative Zephyr® Endobronchial Valve and other products designed to improve the quality of life for COPD patients. The live and archived webcast will be available on Pulmonx's investor website.

Pulmonx to Present at the Canaccord Genuity 46th Annual Growth Conference
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Key Points

  • Pulmonx is showcasing its leadership in COPD treatments at a major growth conference.
  • The company holds FDA Premarket Approval for its Zephyr® Endobronchial Valve, a breakthrough device for emphysema treatment.
  • Pulmonx's products are commercially available in over 25 countries and are recognized in global treatment guidelines.

REDWOOD CITY, Calif., July 28, 2026 (GLOBE NEWSWIRE) -- Pulmonx Corporation (Nasdaq: LUNG) (“Pulmonx”) a global leader in minimally invasive treatments for severe lung disease, today announced the company will be participating in a fireside chat at the Canaccord Genuity 46th Annual Growth Conference in Boston on Tuesday, August 11, 2026, at 1:00 PM PT / 4:00 PM ET.

A live and archived webcast of the fireside chat will be available on “Investors” section of the Pulmonx website at https://investors.pulmonx.com/.

About Pulmonx Corporation
Pulmonx Corporation (Nasdaq: LUNG) is a global leader in minimally invasive treatments for chronic obstructive pulmonary disease (COPD). Pulmonx’s Zephyr® Endobronchial Valve, Chartis® Pulmonary Assessment System, LungTraX® Platform, and StratX® Lung Analysis Reports are designed to assess and treat patients with severe emphysema/COPD who despite medical management are still profoundly symptomatic. Pulmonx received U.S. Food and Drug Administration (FDA) Premarket Approval (PMA) to commercialize the Zephyr® Endobronchial Valve following its designation as a “breakthrough device.” The Zephyr Valve is commercially available in more than 25 countries, is included in global treatment guidelines and is widely considered a standard of care treatment option for improving breathing, activity and quality of life in patients with severe emphysema. For more information on the Zephyr Valves and the company, please visit www.Pulmonx.com.  
  
Pulmonx®, AeriSeal®, Chartis®, LungTraX®, StratX®, and Zephyr® are registered trademarks of Pulmonx Corporation.  

Contact
Brian Johnston
Gilmartin Group
[email protected]


Risks

  • Market acceptance and reimbursement coverage for innovative medical devices like Zephyr® Valve can vary, impacting sales and growth.
  • Regulatory changes or challenges could affect Pulmonx's commercialization efforts and product approvals.
  • Competition from other medical device companies offering alternative COPD treatments may affect market share.

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