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News / Press Release / Research Template | Elementor #8267

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NEWS
PRESS RELEASES
RESEARCH
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Empowering Lung Recovery with Doug Evans of Lungpacer

July 15, 2025

Med Tech Innovation Podcast hosts Kyle Kruse and Richard Meiklejohn interview Lungpacer CEO Doug Evans about the necessary but harmful

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After Tragedy, an Entrepreneur’s Triumph

June 26, 2025

Brian Gormley of the Wall Street Journal publishes article on Lungpacer’s 15-year journey from a deeply personal mission sparked by

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Lungpacer announces 150th global patent for interventional neurostimulation technology portfolio

May 23, 2025

This 150th patent is a testament to our team’s ingenuity and dedication to serving the approximately 2.5 million US patients

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NEWS

Empowering Lung Recovery with Doug Evans of Lungpacer

July 15, 2025

Med Tech Innovation Podcast hosts Kyle Kruse and Richard Meiklejohn interview Lungpacer CEO Doug Evans about the necessary but harmful

Read More

After Tragedy, an Entrepreneur’s Triumph

June 26, 2025

Brian Gormley of the Wall Street Journal publishes article on Lungpacer’s 15-year journey from a deeply personal mission sparked by

Read More

Lungpacer announces 150th global patent for interventional neurostimulation technology portfolio

May 23, 2025

This 150th patent is a testament to our team’s ingenuity and dedication to serving the approximately 2.5 million US patients

Read More
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PRESS RELEASES

Lungpacer to Showcase the Potential of Novel Technologies to Improve Lung, Heart, and Brain Health in Ventilated Patients

April 28, 2025

Exton, PA – April 28, 2025 – This spring, Lungpacer Medical clinical experts and device innovators will be featured presenters

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Kevin Kearney Joins Lungpacer Medical as Chief Commercial Officer

March 24, 2025

Company Appoints Medical Device and Healthcare Industry Veteran with 20 Years of Experience Exton, PA – March 24, 2025 –

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Lungpacer Medical Announces Investigational Device Exemption (IDE) for STARI, Phase 2 Feasibility Clinical Trial 

March 10, 2025

Exton, PA – March 10, 2025 – Lungpacer Medical, a leading neurostimulation company committed to advancing therapies that assist patients

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RESEARCH

June 2025 | American Journal of Respiratory and Critical Care Medicine (AJRCCM) | Temporary Transvenous Diaphragm Neurostimulation for Weaning from Mechanical Ventilation (RESCUE-3)

June 12, 2025
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May 2025 | Critical Care | Phrenic stimulation decreases brain injury biomarkers in sedated mechanically ventilated patients: preliminary observations

May 27, 2025
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April 2025 | Cardiovascular Research Foundation THT | Diaphragm Neurostimulation to optimize Biventricular Performance during Invasive Mechanical Ventilation for Acute Respiratory Failure

April 8, 2025
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© 2024 Lungpacer Medical Inc. ®

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AEROPACE SYSTEM INDICATIONS FOR USE

The AeroPace System is indicated to improve weaning success – increase weaning, reduce ventilator days, and reduce reintubation – in patients ages 18 years or older on mechanical ventilation ≥ 96 hours and who have not weaned.

SAFETY INFORMATION

Do not use the AeroPace System with active implanted cardiac pacemakers, defibrillators, or other implantable electronics within proximity to the AeroPace Neurostimulation Catheter. The AeroPace System has not been clinically evaluated for safety with these implantable electronic devices.

Risks include those that may occur with the use of central venous catheters and the risks of nerve and diaphragm stimulation.  These may include the risks of infection, blood vessel damage, or cardiac effects that can occur with use of catheters.  Stimulation risks are rare and may include nerve injury or fatigue of the breathing muscle.

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CAUTION: The AeroNova System is limited by Federal law (United States) to investigational use. Used exclusively for clinical investigations.

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Lungpacer® Medical, AeroPace® System and AeroNova® System are registered trademarks of Lungpacer Medical.

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The AeroPace® System is approved by the United States Food and Drug Administration to improve weaning success in adult patients on mechanical ventilation at least 96 hours and who have not weaned. The AeroPace System is not approved in any other country.

The AeroNova® System is limited by Federal Law (United States)to investigational use. Used exclusively for clinical investigations.

Lungpacer is developing innovative new technologies. By visiting Lungpacer Medical’s website, you acknowledge that not all the technology cited has regulatory approval and clinical trials are ongoing for investigational devices. These clinical studies may show an increased benefit, no benefit, or an adverse benefit to the patient.

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