Pulmonx Corporation

FDA Regulatory Profile

Pulmonx Corporation appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 13, 2026.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K253096Chartis Precision CatheterFebruary 13, 2026
K222340Chartis Precision CatheterDecember 1, 2022
K212494Lung Image AnalysisSeptember 2, 2021
K180011Pulmonx Chartis Tablet ConsoleJuly 13, 2018