Pulmonx Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pulmonx Corporation - FDA 510(k) Cleared Devices
Recent clearances: Chartis Precision Catheter, Chartis Precision Catheter, Lung Image Analysis
4
Total
4
Cleared
0
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.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Pulmonx Corporation
4 devices