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Pulmonx Corporation

United States·US-MF-000038432

Last updated May 30, 2026

Information

Country: United States
Address: 700, Chesapeake Drive, Redwood City, United States
Website: pulmonx.com/about-pulmonx/
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: +1 650 364 0400
PRRC Contact: Rizwan Pervez
EUDAMED SRN: US-MF-000038432
FDA FEI Number: —
DUNS Number: 958582595

Catalogue (26)

Device	Model / Reference	Registries	Class	Status
Zephyr Delivery Catheter	EDC-TS-5.5	FDA UDI	Class III	Active
Chartis Console	G3	FDA UDI	Class II	Active
Pulmonx Chartis Tablet Console	CHR-CO-300	FDA UDI	Class II	Active
Zephyr Delivery Catheter	EDC-TS-4.0	FDA UDI	Class III	Active
Zephyr Endobronchial Valve	EBV-TS-5.5-LP	FDA UDI	Class III	Active
Lung Image Analysis	LIA-01-001	FDA UDI	Class II	Active
Chartis Catheter	G3	FDA UDI	Class II	Active
Chartis Catheter	G3	FDA UDI	Class II	Active
Zephyr Endobronchial Valve	EBV-TS-4.0-LP	FDA UDI	Class III	Active
Zephyr Endobronchial Valve	EBV-TS-4.0	FDA UDI	Class III	Active
Zephyr Delivery Catheter	EDC-TS-4.0-J	FDA UDI	Class III	Active
Pulmonx Chartis Tablet Console	CHR-CO-300	FDA UDI	Class II	Active
Zephyr Delivery Catheter	EDC-TS-5.5-DM	FDA UDI	Class III	Active
Zephyr Endobronchial Valve	EBV-TS-5.5	FDA UDI	Class III	Active
Chartis Precision Catheter	G4	FDA UDI	Class II	Active
Pulmonx Chartis Tablet Console	K180011	FDA 510(k)	Class II	Active
Lung Image Analysis	K212494	FDA 510(k)	Class II	Active
Chartis Precision Catheter	K222340	FDA 510(k)	Class II	Active
Chartis Precision Catheter	K253096	FDA 510(k)	Class II	Active
The Visualized Endotracheal Tube System Or Vett System	K973191	FDA 510(k)	Class II	Active
Chartis Console	K083199	FDA 510(k)	Class II	Active
Chartis Catheter Model Chr-Ca-12.0	K111522	FDA 510(k)	Class II	Active
Chartis Console	K111764	FDA 510(k)	Class II	Active
Chartis Pulmonary Assessment System Catheter	CHR-CA-12.0	EUDAMED	Class IIa	Active
Chartis Pulmonary Assessment Catheter XL	CHR-CA-12.0-XL	EUDAMED	Class IIa	Active
Zephyr Endobronchial Valve (EBV) System	P180002	FDA PMA	Class III	Active

Related Companies

Authorised Representatives

Pulmonx GmbH DE

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (1)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
Aug 31, 2023	Z-0235-2024	—	open, classified	Endobronchial implant devices may have been labeled with a shortened expiration date but they can be used until the correct expiration date: 08 December 2024.