PULMONX, Corp.
1 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (1)
- Inspections (2)
Devices registered here (1)
- Spirometer, DiagnosticProduct code BZG (opens in a new tab) · Class II · Anesthesiology · 21 CFR 868.1840
Recalls & enforcement
- Class IIOngoing2023-08-31Endobronchial implant devices may have been labeled with a shortened expiration date but they can be used until the correct expiration date: 08 December 2024.
FDA inspections (2)
- NAI2026-07-02No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
- VAI2016-11-08Voluntary Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.
Related
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “PULMONX, Corp. (FEI 3007797756) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3007797756-pulmonx-corp/
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