Press Releases August 27, 2026 04:05 PM

Pulmonx to Participate in Upcoming Investor Conferences

Pulmonx announces management participation in upcoming healthcare investor conferences

By Avery Klein
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Pulmonx Corporation, a Nasdaq-listed company specializing in minimally invasive treatments for severe lung disease, will have its management team participate in two major investor conferences in September 2026. The company's products, including the FDA-approved Zephyr® Endobronchial Valve, are recognized in global treatment guidelines for severe emphysema/COPD, supporting improved patient outcomes.

Pulmonx to Participate in Upcoming Investor Conferences
LUNG
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Key Points

  • Pulmonx will attend the Wells Fargo Healthcare Conference and the Lake Street Best Ideas Growth Conference in September.
  • The company’s Zephyr® Endobronchial Valve holds FDA Premarket Approval and is a breakthrough device for treating severe emphysema and COPD.
  • Pulmonx’s innovative products are commercially available globally and integrated into treatment standards for lung disease.
  • Sectors impacted include healthcare technology, medical devices, and biotechnology focusing on respiratory diseases.

REDWOOD CITY, Calif., Aug. 27, 2026 (GLOBE NEWSWIRE) -- Pulmonx Corporation (Nasdaq: LUNG) (“Pulmonx”) a global leader in minimally invasive treatments for severe lung disease, today announced that management will participate in the following upcoming investor conferences:

Wells Fargo Healthcare Conference
Format: 1x1 meetings
Date: Wednesday, September 9
Location: Boston, MA

Lake Street Best Ideas Growth (BIG10) Conference
Format: 1x1 meetings
Date: Thursday, September 10
Location: New York, NY

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 or Webb Campbell
Gilmartin Group
investors@pulmonx.com


Risks

  • Attendance at investor conferences does not guarantee positive financial performance or investor interest.
  • Market acceptance and ongoing regulatory approvals remain critical for commercial success in the medical device sector.
  • Competition and technological advances in COPD treatment could impact Pulmonx’s market position.

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