Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA PMA

Normothermic preservation system for transplantation of initially unacceptable donor lungs

PMA Number: P240033 · 2026-06-22

ApplicantLung Bioengineering, Inc.
Decision Date2026-06-22
PMA NumberP240033
Product CodePHO
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeGU

Device Summary

Normothermic preservation system for transplantation of initially unacceptable donor lungs is the device name listed in this FDA 510(k) record. The listed applicant is Lung Bioengineering, Inc.. It received FDA 510(k) clearance on 2026-06-22. The device is classified under product code PHO. It was reviewed by the GU advisory panel.

Frequently Asked Questions

What is the Normothermic preservation system for transplantation of initially unacceptable donor lungs?

Normothermic preservation system for transplantation of initially unacceptable donor lungs is a medical device that received FDA 510(k) clearance on 2026-06-22. The listed applicant is Lung Bioengineering, Inc..

When did Normothermic preservation system for transplantation of initially unacceptable donor lungs receive FDA 510(k) clearance?

The clearance date for Normothermic preservation system for transplantation of initially unacceptable donor lungs can be found in the official FDA records.

Who is the listed applicant for Normothermic preservation system for transplantation of initially unacceptable donor lungs?

The FDA 510(k) record lists Lung Bioengineering, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Normothermic preservation system for transplantation of initially unacceptable donor lungs?

The FDA product code for Normothermic preservation system for transplantation of initially unacceptable donor lungs is PHO.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑