Pulmonx Corporation - FDA 510(k) Cleared Devices

Pulmonx Corporation has 4 FDA 510(k) cleared medical devices. Based in Redwood Citry, US.

Latest FDA clearance: Feb 2026. Active since 2018. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Pulmonx Corporation Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.