Press Releases July 15, 2026 04:05 PM

Pulmonx to Report Second Quarter 2026 Financial Results on July 29, 2026

Pulmonx to announce Q2 2026 financial results on July 29 with a follow-up conference call

By Derek Hwang
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Pulmonx Corporation, a Nasdaq-listed company specializing in minimally invasive treatments for lung disease, announced it will release its second quarter 2026 financial results on July 29, 2026, followed by a management conference call. The company is known for its Zephyr Endobronchial Valve and related pulmonary assessment technologies aimed at treating severe emphysema and COPD.

Pulmonx to Report Second Quarter 2026 Financial Results on July 29, 2026
LUNG
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Key Points

  • Pulmonx will report Q2 2026 financial results after market close on July 29, 2026.
  • Management will hold a conference call to discuss the results, accessible via webcast.
  • Pulmonx's products, including the Zephyr Valve, are FDA-approved and globally recognized standards for treating severe emphysema and COPD.
  • Impacted sectors include healthcare, biomedical technology, and medical devices, particularly in respiratory treatment and chronic disease management.

REDWOOD CITY, Calif., July 15, 2026 (GLOBE NEWSWIRE) -- Pulmonx Corporation (Nasdaq: LUNG) (“Pulmonx”), a global leader in minimally invasive treatments for lung disease, today announced that it will release financial results for the second quarter of 2026 after the close of trading on Wednesday, July 29, 2026. Company management will host a conference call to discuss financial results beginning at 1:30 p.m. PT / 4:30 p.m. ET.

A live and archived webcast of the event will be available on the “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 and StratX® Lung Analysis Platform 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®, Chartis®, StratX®, and Zephyr® are registered trademarks of Pulmonx Corporation.

Contact
Brian Johnston or Webb Campbell
Gilmartin Group
[email protected]


Risks

  • Financial results could reveal performance below market expectations, impacting stock price.
  • Regulatory changes or reimbursement challenges in healthcare could affect product commercialization.
  • Competition in the respiratory medical device market may pressure growth and market share.

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