Press Releases April 28, 2026 04:05 PM

Pulmonx to Present at the Bank of America Securities 2026 Health Care Conference

Pulmonx to present at major healthcare conference highlighting advancements in COPD treatment

By Caleb Monroe
Share
Twitter Reddit Facebook LinkedIn
LUNG

Pulmonx Corporation announced it will present at the Bank of America Securities 2026 Health Care Conference, showcasing its leadership in minimally invasive treatments for severe lung disease, especially COPD, with FDA-approved products like the Zephyr Endobronchial Valve that improve patient outcomes globally.

Pulmonx to Present at the Bank of America Securities 2026 Health Care Conference
LUNG
Summarize with
ChatGPT Perplexity Claude Grok Gemini

Key Points

  • Pulmonx will present at a prominent healthcare investor conference, increasing visibility among investors and analysts.
  • The company is a global leader in minimally invasive treatments for severe COPD with FDA pre-market approval for the Zephyr Valve, marketed in over 25 countries.
  • Pulmonx's products are recognized in global treatment guidelines and have a strong reputation for improving quality of life in emphysema patients.
  • Sectors impacted include healthcare, biotechnology, and medical devices, particularly those focusing on respiratory diseases.

REDWOOD CITY, Calif., April 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 presenting at the Bank of America Securities 2026 Health Care Conference in Las Vegas on Tuesday, May 12, 2026, at 8:15 AM PT / 11:15 AM ET.

A live and archived webcast of the presentation 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, LungTraXTM 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 FDA pre-market approval to commercialize the Zephyr 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®, StratX®, and Zephyr® are registered trademarks and LungTraXTM is a trademark of Pulmonx Corporation. 

Contact
Brian Johnston
Gilmartin Group
[email protected]


Risks

  • Success depends on continued regulatory approvals and market adoption of Pulmonx's products, which could be affected by competitive medical technologies.
  • Market volatility and investor sentiment towards biotech stocks could impact stock performance regardless of clinical progress.
  • Any failure to meet financial or clinical expectations announced during the presentation could negatively affect the stock price.

More from Press Releases

Agios Showcases RISE UP Phase 3 Results at EHA 2026 Plenary Session Reinforcing Strong Anti-Hemolytic Profile of Mitapivat in Sickle Cell Disease Jun 13, 2026 Rhythm Pharmaceuticals Presents Positive Interim Six-month Data from Phase 2 Trial of Setmelanotide in Patients with Prader-Willi Syndrome (PWS) at ENDO 2026 Jun 13, 2026 Intellia Therapeutics Reports Additional Positive Phase 3 Results for Lonvoguran Ziclumeran (lonvo-z) in Patients with Hereditary Angioedema Jun 13, 2026 Arcadia Biosciences (RKDA) Announces Closing of $4 Million Private Placement Priced At-The-Market Under Nasdaq Rules Jun 12, 2026 Belite Bio Completes Rolling Submission of New Drug Application to U.S. Food and Drug Administration for Tinlarebant for the Treatment of Stargardt Disease Type 1 Jun 12, 2026