Medical Device Manufacturer · US , Redwood Citry , CA

Pulmonx Corporation - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2018

Total

Cleared

Denied

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.

FDA 510(k) cleared devices by Pulmonx Corporation

4 devices

1-4 of 4