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Lungpacer Medical

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uuid0000vo9

Namestring
Lungpacer Medical
Legal namestring
Lungpacer Medical Inc.
Websiteurl
lungpacer.com
Company typeenum
Private
Founded yearint
2009
Descriptiontext

Lungpacer Medical is a privately held medical device company founded in 2009 as a Simon Fraser University spinout, headquartered in Vancouver, Canada with U.S. operations based in Exton, Pennsylvania. The company develops temporary transvenous diaphragm neurostimulation (TTDN) systems that stimulate the phrenic nerves via a catheter-based approach to activate and strengthen the diaphragm in mechanically ventilated adult patients, addressing diaphragm atrophy (which can reach 50% within one day of mechanical ventilation) and weaning failure. Its flagship product, the AeroPace System, received FDA Premarket Approval in December 2024 and is indicated to improve weaning success in patients aged 18+ on mechanical ventilation for 96+ hours who have failed to wean; the system consists of an airway pressure sensor, a touchscreen neurostimulation console, and a temporary transvenous catheter with 30 specialized electrodes in two arrays delivering two sets of 60 stimulations daily. A next-generation AeroNova system is in Phase 2 (STARI) feasibility trials and a SupAira application targets organ donor lung management, both backed by BARDA funding and the DONATE study respectively.

The company sells the AeroPace System directly to U.S. hospitals through a field sales organization that includes clinical specialists and reimbursement support staff, with CMS NTAP approval (effective October 1, 2025) enabling up to $23,650.90 in additional Medicare reimbursement per case under the new ICD-10-PCS code X2H13XB. Its go-to-market is enterprise field sales targeted at ICU and critical care departments at major U.S. medical centers, complemented by clinical conference presentations (AJRCCM publication, ATS, THT, Critical Care Reviews Meeting, American Transplant Congress) and earned media including a Wall Street Journal profile. Revenue is generated primarily from hardware sales (neurostimulation console plus single-patient-use catheter) with bundled clinical training and reimbursement support services. The company is led by CEO Doug Evans and a management team with track records of medtech exits at Kensey Nash, Intact Vascular, Ventec Life Systems, and Ceribell, and has raised approximately $150M+ across disclosed funding rounds since inception.

Short descriptiontext

Lungpacer Medical is a Vancouver-based medical device company that develops FDA-approved temporary transvenous diaphragm neurostimulation systems (AeroPace) to help mechanically ventilated adults wean from ventilation by activating and strengthening the diaphragm, selling directly to U.S. hospital ICUs.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
51–100
akta.pro rankint
HeadquartersVancouver, Canada
HQ citystring
Vancouver
HQ countrystring
Canada
HQ regionstring
North America
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
diaphragm neurostimulation devices, ventilator weaning systems, respiratory medical devices, critical care neurostimulation, mechanical ventilation therapy
Industry3 codes
1Anesthesia & Airway Management Equipment (Workstations, Laryngoscopy, Ventilation adjuncts)
CodeHLAHADAJPrimaryYes
2Ventilators & Mechanical Ventilation Systems (ICU/Transport/Home)
CodeHLAHAGACPrimaryNo
3Home Ventilation, Oxygen Therapy & Respiratory DME Clinical Management
CodeHLAKANAMPrimaryNo
NAICS code2 codes
  • Surgical and Medical Instrument Manufacturing339112
  • Surgical Appliance and Supplies Manufacturing339113
SIC code2 codes
  • Electromedical & Electrotherapeutic Apparatus3845
  • Surgical & Medical Instruments & Apparatus3841
Product category
Respiratory / Critical Care Medical Devices
GTM motion3 records

Each record includes

Type, Description, Source

Revenue model2 records
1AeroPace Neurostimulation System (Hardware + Procedure)
TypeHardware Sales
Description

Revenue is generated from the sale of the AeroPace Neurostimulation System hardware (neurostimulation console and temporary transvenous catheter) to hospitals for use in ICU settings. The system is a single-patient-use device. Hospitals receive CMS NTAP reimbursement of up to $23,650.90 per eligible case under Medicare, and Lungpacer captures revenue from hospital procurement of the system and consumables.

lungpacer.com
2Professional Services and Clinical Support
TypeProfessional Services
Description

Lungpacer provides clinical training, reimbursement support, and field clinical specialist services to hospitals adopting the AeroPace system, supporting successful implementation and utilization.

lungpacer.com
Marketing channels8 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels2 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Personnel, Technology or R&D, Marketing or Sales, Supply Chain, Operations
Pricing details1 tier
1AeroPace System Medicare NTAP Reimbursement
ModelOtherBilling cadencePay-as-you-go
Notes

Hospitals eligible for up to $23,650.90 in additional Medicare reimbursement per case via CMS New Technology Add-on Payment (NTAP), representing up to 65% of the additional cost of the technology. Effective October 1, 2025 under FY2026 IPPS Final Rule.

lungpacer.com
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 3 records shown
1AeroPace System
Description

FDA-approved temporary transvenous diaphragm neurostimulation system for mechanically ventilated patients to improve weaning success

lungpacer.com
+2 more records
Core offering1 text field

Lungpacer Medical develops and sells the AeroPace Neurostimulation System, an FDA-approved temporary transvenous diaphragm neurostimulation (TTDN) device that stimulates the phrenic nerves via a catheter-based approach to activate and strengthen the diaphragm in adult patients on prolonged mechanical ventilation (≥96 hours) who have failed to wean. The system comprises three components (airway pressure sensor, touchscreen neurostimulation console, and temporary transvenous catheter with 30 electrodes) that integrate into existing ICU workflows without surgical implantation. The company is also developing next-generation AeroNova and SupAira systems extending the platform to earlier-stage ventilation and organ donor management.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 9 values shown
  • 43% faster weaning from mechanical ventilation over 30 days
+8 more records
Product overview1 text field

Lungpacer Medical offers a portfolio of neurostimulation-based medical devices designed to address diaphragm dysfunction in critically ill patients. The flagship product is the FDA-approved AeroPace System, a temporary transvenous diaphragm neurostimulation device that helps mechanically ventilated patients wean from ventilation by stimulating the phrenic nerves to strengthen the diaphragm. The portfolio includes the investigational AeroNova System for continual diaphragm neurostimulation during mechanical ventilation, and the SupAira System application for organ donor management. The AeroPace System integrates three components (airway pressure sensor, neurostimulation console, and temporary transvenous catheter) that work with standard ventilators in ICU workflows.

Product and service3 records
1AeroPace Neurostimulation System
CategoryCritical Care Neurostimulation Device
Description

FDA-approved temporary transvenous diaphragm neurostimulation (TTDN) system that stimulates the phrenic nerves via a catheter-based approach to activate and strengthen the diaphragm in adult patients on mechanical ventilation for ≥96 hours who have failed to wean. Comprises an airway pressure sensor, touchscreen neurostimulation console, and temporary transvenous catheter with 30 specialized electrodes in two arrays. Indicated for hospital ICU use.

2AeroNova System
CategoryInvestigational Critical Care Neurostimulation Device
Description

Investigational next-generation continual diaphragm neurostimulation system designed to deliver therapy in conjunction with mechanical ventilation at reduced positive pressures, intended to mitigate multi-organ ventilator-induced injury (diaphragm, cardiac, and brain) from the earliest stages of mechanical ventilation. Currently in Phase 2 STARI clinical trial.

3SupAira System
CategoryOrgan Donor Management Neurostimulation Device
Description

Application of Lungpacer's transvenous neurostimulation technology for respiratory management of brain-dead organ donors, using temporary transvenous phrenic nerve stimulation to activate the diaphragm during donor management in order to improve oxygenation, reduce atelectasis, and increase transplantable lung yield.

Scale indicator9 records

Each record includes

Type, Value, Description, Source

Partnership1 partner
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-06-23
Description

Mid-America Transplant in St. Louis, MO served as the research partner for the DONATE clinical study evaluating SupAira diaphragm neurostimulation in 50 brain-dead organ donors. Gary F. Marklin, MD, Chief Medical and Research Officer at Mid-America Transplant, presented the DONATE findings at the American Transplant Congress 2026. The study demonstrated that diaphragm neurostimulation significantly increased donor lungs meeting transplant criteria compared to matched contemporary controls.

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeEmerging player
Description

TransMedics is a leader in organ transplant logistics and ex-vivo organ perfusion. While its technology differs from Lungpacer's SupAira diaphragm neurostimulation, both companies target the lung transplant ecosystem — TransMedics via organ preservation, Lungpacer via improving donor lung utilization through neurostimulation.

TypeDirect peer
Description

Synapse Biomedical manufactures the NeuRx Diaphragm Pacing System (DPS), a phrenic nerve stimulation device for diaphragm conditioning. While NeuRx requires surgical laparoscopic implantation versus Lungpacer's transvenous approach, it is the most direct competing technology for diaphragm neurostimulation in ventilated patients.

TypeDirect peer
Description

Avery Biomedical Devices produces implantable diaphragm pacemakers (Mark IV Breathing Pacemaker) that stimulate the phrenic nerve, primarily for spinal cord injury and central sleep apnea patients. It competes in the broader diaphragm neurostimulation category though its surgical implant approach differs from Lungpacer's catheter-based temporary system.

TypeBroad incumbent
Description

Medtronic has historically been a leading player in diaphragm pacing through its acquisition of Synapse Biomedical-related IP and has a broad respiratory and ICU portfolio. As a major medtech incumbent with deep hospital relationships, it represents both a potential competitor and a strategic acquirer for the diaphragm neurostimulation category.

TypeBroad incumbent
Description

Getinge is a global leader in ICU ventilation with products like the Servo-i and Servo-u ventilator platforms used in critical care. As a dominant ventilator supplier, Getinge is a natural channel partner or potential competitor in advanced respiratory care adjuncts targeting mechanically ventilated patients.

TypeBroad incumbent
Description

Dräger is a major manufacturer of ICU ventilators (Evita, Oxylog, Babylog families) and acute care equipment. Its installed base in critical care units globally makes it a relevant incumbent that could expand into diaphragm neurostimulation adjuncts or partner with Lungpacer for ventilator-integrated solutions.

TypeBroad incumbent
Description

Hamilton Medical manufactures intelligent ICU ventilators (HAMILTON-C1, G5, C6) with a global footprint in critical care. Its installed base and ICU integration expertise position it as an incumbent comparable to Lungpacer's customer-facing environment, though it does not currently offer a diaphragm neurostimulation product.

TypeBroad incumbent
Description

Vyaire Medical is a respiratory care company offering ventilators (Bellavista, Avea) and respiratory diagnostics. Its focus on the ICU ventilation market and broad product portfolio make it a relevant comparable for companies selling into critical care departments.

TypeBroad incumbent
Description

Philips, through its Respironics franchise, has been a leading player in respiratory care including non-invasive ventilation and hospital ventilation. Its scale and hospital relationships make it a meaningful comparable in the broader ICU respiratory care market, even though it does not currently offer diaphragm neurostimulation.

TypeEmerging player
Description

Inspire Medical Systems commercializes an implantable neurostimulation device for obstructive sleep apnea. While it targets a different patient population (sleep apnea vs. ICU weaning), it is a relevant comparable as a neurostimulation-based medical device company that built a successful commercial franchise around pharyngeal nerve stimulation.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat5 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers1 record

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment3 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile2 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature6 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles12 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

Subsidiaries1 record

Each record includes

Name, Acquired on, Relationship type, Type, Business focus

Compliance2 records

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds10 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors4 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Lungpacer Medical

Respiratory / Critical Care Medical Deviceslungpacer.com

Lungpacer Medical is a Vancouver-based medical device company that develops FDA-approved temporary transvenous diaphragm neurostimulation systems (AeroPace) to help mechanically ventilated adults wean from ventilation by activating and strengthening the diaphragm, selling directly to U.S. hospital ICUs.

What Lungpacer Medical does

Lungpacer Medical is a privately held medical device company founded in 2009 as a Simon Fraser University spinout, headquartered in Vancouver, Canada with U.S. operations based in Exton, Pennsylvania. The company develops temporary transvenous diaphragm neurostimulation (TTDN) systems that stimulate the phrenic nerves via a catheter-based approach to activate and strengthen the diaphragm in mechanically ventilated adult patients, addressing diaphragm atrophy (which can reach 50% within one day of mechanical ventilation) and weaning failure. Its flagship product, the AeroPace System, received FDA Premarket Approval in December 2024 and is indicated to improve weaning success in patients aged 18+ on mechanical ventilation for 96+ hours who have failed to wean; the system consists of an airway pressure sensor, a touchscreen neurostimulation console, and a temporary transvenous catheter with 30 specialized electrodes in two arrays delivering two sets of 60 stimulations daily. A next-generation AeroNova system is in Phase 2 (STARI) feasibility trials and a SupAira application targets organ donor lung management, both backed by BARDA funding and the DONATE study respectively.

The company sells the AeroPace System directly to U.S. hospitals through a field sales organization that includes clinical specialists and reimbursement support staff, with CMS NTAP approval (effective October 1, 2025) enabling up to $23,650.90 in additional Medicare reimbursement per case under the new ICD-10-PCS code X2H13XB. Its go-to-market is enterprise field sales targeted at ICU and critical care departments at major U.S. medical centers, complemented by clinical conference presentations (AJRCCM publication, ATS, THT, Critical Care Reviews Meeting, American Transplant Congress) and earned media including a Wall Street Journal profile. Revenue is generated primarily from hardware sales (neurostimulation console plus single-patient-use catheter) with bundled clinical training and reimbursement support services. The company is led by CEO Doug Evans and a management team with track records of medtech exits at Kensey Nash, Intact Vascular, Ventec Life Systems, and Ceribell, and has raised approximately $150M+ across disclosed funding rounds since inception.

Lungpacer Medical firmographics

Firmographics
Name
Lungpacer Medical
Legal name
Lungpacer Medical Inc.
Website
https://lungpacer.com
Company type
Private
Founded year
2009
Operating status
Operating
Headcount range
51–100 employees
Short description
Lungpacer Medical is a Vancouver-based medical device company that develops FDA-approved temporary transvenous diaphragm neurostimulation systems (AeroPace) to help mechanically ventilated adults wean from ventilation by activating and strengthening the diaphragm, selling directly to U.S. hospital ICUs.
Ownership category
akta.pro rank

Lungpacer Medical industry classification

Industry
Product category
Respiratory / Critical Care Medical Devices
NAICS
Surgical and Medical Instrument Manufacturing (339112), Surgical Appliance and Supplies Manufacturing (339113)
SIC
Electromedical & Electrotherapeutic Apparatus (3845), Surgical & Medical Instruments & Apparatus (3841)
akta.pro primary industry
Anesthesia & Airway Management Equipment (Workstations, Laryngoscopy, Ventilation adjuncts) (HLAHADAJ)
akta.pro secondary industries
Ventilators & Mechanical Ventilation Systems (ICU/Transport/Home) (HLAHAGAC), Home Ventilation, Oxygen Therapy & Respiratory DME Clinical Management (HLAKANAM)

Keywords

  • Diaphragm neurostimulation devices
  • Ventilator weaning systems
  • Respiratory medical devices
  • Critical care neurostimulation
  • Mechanical ventilation therapy

Where Lungpacer Medical is headquartered

Location

Headquarters

HQ city
Vancouver
HQ country
Canada
HQ region
North America

Offices2 records

Markets served

Lungpacer Medical business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Personnel, Technology or R&D, Marketing or Sales, Supply Chain, Operations

Revenue model

  1. AeroPace Neurostimulation System (Hardware + Procedure): Revenue is generated from the sale of the AeroPace Neurostimulation System hardware (neurostimulation console and temporary transvenous catheter) to hospitals for use in ICU settings. The system is a single-patient-use device. Hospitals receive CMS NTAP reimbursement of up to $23,650.90 per eligible case under Medicare, and Lungpacer captures revenue from hospital procurement of the system and consumables.
  2. Professional Services and Clinical Support: Lungpacer provides clinical training, reimbursement support, and field clinical specialist services to hospitals adopting the AeroPace system, supporting successful implementation and utilization.

Pricing tiers

ModelBillingPrice
OtherPay-as-you-goAeroPace System Medicare NTAP Reimbursement

Go-to-market motion3 records

Distribution channels2 records

Marketing channels8 records

Lungpacer Medical product offering

Product offering

Core offering

Lungpacer Medical develops and sells the AeroPace Neurostimulation System, an FDA-approved temporary transvenous diaphragm neurostimulation (TTDN) device that stimulates the phrenic nerves via a catheter-based approach to activate and strengthen the diaphragm in adult patients on prolonged mechanical ventilation (≥96 hours) who have failed to wean. The system comprises three components (airway pressure sensor, touchscreen neurostimulation console, and temporary transvenous catheter with 30 electrodes) that integrate into existing ICU workflows without surgical implantation. The company is also developing next-generation AeroNova and SupAira systems extending the platform to earlier-stage ventilation and organ donor management.

Product overview

Lungpacer Medical offers a portfolio of neurostimulation-based medical devices designed to address diaphragm dysfunction in critically ill patients. The flagship product is the FDA-approved AeroPace System, a temporary transvenous diaphragm neurostimulation device that helps mechanically ventilated patients wean from ventilation by stimulating the phrenic nerves to strengthen the diaphragm. The portfolio includes the investigational AeroNova System for continual diaphragm neurostimulation during mechanical ventilation, and the SupAira System application for organ donor management. The AeroPace System integrates three components (airway pressure sensor, neurostimulation console, and temporary transvenous catheter) that work with standard ventilators in ICU workflows.

Differentiator

Problem solved

Functional benefit

Brands

  • AeroPace System: FDA-approved temporary transvenous diaphragm neurostimulation system for mechanically ventilated patients to improve weaning success
  • AeroNova System
  • SupAira System

Products and services

  • AeroPace Neurostimulation System FDA-approved temporary transvenous diaphragm neurostimulation (TTDN) system that stimulates the phrenic nerves via a catheter-based approach to activate and strengthen the diaphragm in adult patients on mechanical ventilation for ≥96 hours who have failed to wean. Comprises an airway pressure sensor, touchscreen neurostimulation console, and temporary transvenous catheter with 30 specialized electrodes in two arrays. Indicated for hospital ICU use.
  • AeroNova System Investigational next-generation continual diaphragm neurostimulation system designed to deliver therapy in conjunction with mechanical ventilation at reduced positive pressures, intended to mitigate multi-organ ventilator-induced injury (diaphragm, cardiac, and brain) from the earliest stages of mechanical ventilation. Currently in Phase 2 STARI clinical trial.
  • SupAira System Application of Lungpacer's transvenous neurostimulation technology for respiratory management of brain-dead organ donors, using temporary transvenous phrenic nerve stimulation to activate the diaphragm during donor management in order to improve oxygenation, reduce atelectasis, and increase transplantable lung yield.

Quantifiable outcome

  • 43% faster weaning from mechanical ventilation over 30 days
  • +8 more outcomes

Companies that use Lungpacer Medical

Customer profile

Named customers1 record

Segments3 records

Ideal customer profiles2 records

Lungpacer Medical technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature6 records

Lungpacer Medical partnerships and signals

Strategic signal

Partnerships

One partnership is on record.

  • Mid-America TransplantcoreStrategic or Co-development Partner · 23 June 2026Mid-America Transplant in St. Louis, MO served as the research partner for the DONATE clinical study evaluating SupAira diaphragm neurostimulation in 50 brain-dead organ donors. Gary F. Marklin, MD, Chief Medical and Research Officer at Mid-America Transplant, presented the DONATE findings at the American Transplant Congress 2026. The study demonstrated that diaphragm neurostimulation significantly increased donor lungs meeting transplant criteria compared to matched contemporary controls.

Scale indicators9 records

Recent moves7 records

Expansion highlights6 records

Lungpacer Medical competitors and assessment

Company assessment

Emerging players

  • TransMedics: TransMedics is a leader in organ transplant logistics and ex-vivo organ perfusion. While its technology differs from Lungpacer's SupAira diaphragm neurostimulation, both companies target the lung transplant ecosystem — TransMedics via organ preservation, Lungpacer via improving donor lung utilization through neurostimulation.
  • Inspire Medical Systems: Inspire Medical Systems commercializes an implantable neurostimulation device for obstructive sleep apnea. While it targets a different patient population (sleep apnea vs. ICU weaning), it is a relevant comparable as a neurostimulation-based medical device company that built a successful commercial franchise around pharyngeal nerve stimulation.

Direct peers

  • Synapse Biomedical: Synapse Biomedical manufactures the NeuRx Diaphragm Pacing System (DPS), a phrenic nerve stimulation device for diaphragm conditioning. While NeuRx requires surgical laparoscopic implantation versus Lungpacer's transvenous approach, it is the most direct competing technology for diaphragm neurostimulation in ventilated patients.
  • Avery Biomedical Devices: Avery Biomedical Devices produces implantable diaphragm pacemakers (Mark IV Breathing Pacemaker) that stimulate the phrenic nerve, primarily for spinal cord injury and central sleep apnea patients. It competes in the broader diaphragm neurostimulation category though its surgical implant approach differs from Lungpacer's catheter-based temporary system.

Broad incumbents

  • Medtronic: Medtronic has historically been a leading player in diaphragm pacing through its acquisition of Synapse Biomedical-related IP and has a broad respiratory and ICU portfolio. As a major medtech incumbent with deep hospital relationships, it represents both a potential competitor and a strategic acquirer for the diaphragm neurostimulation category.
  • Getinge: Getinge is a global leader in ICU ventilation with products like the Servo-i and Servo-u ventilator platforms used in critical care. As a dominant ventilator supplier, Getinge is a natural channel partner or potential competitor in advanced respiratory care adjuncts targeting mechanically ventilated patients.
  • Dräger: Dräger is a major manufacturer of ICU ventilators (Evita, Oxylog, Babylog families) and acute care equipment. Its installed base in critical care units globally makes it a relevant incumbent that could expand into diaphragm neurostimulation adjuncts or partner with Lungpacer for ventilator-integrated solutions.
  • Hamilton Medical: Hamilton Medical manufactures intelligent ICU ventilators (HAMILTON-C1, G5, C6) with a global footprint in critical care. Its installed base and ICU integration expertise position it as an incumbent comparable to Lungpacer's customer-facing environment, though it does not currently offer a diaphragm neurostimulation product.
  • Vyaire Medical: Vyaire Medical is a respiratory care company offering ventilators (Bellavista, Avea) and respiratory diagnostics. Its focus on the ICU ventilation market and broad product portfolio make it a relevant comparable for companies selling into critical care departments.
  • Philips Respironics: Philips, through its Respironics franchise, has been a leading player in respiratory care including non-invasive ventilation and hospital ventilation. Its scale and hospital relationships make it a meaningful comparable in the broader ICU respiratory care market, even though it does not currently offer diaphragm neurostimulation.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat5 records

Key risks6 records

Key highlights7 records

Customer concentration

Lungpacer Medical social profiles

Digital presence

Lungpacer Medical compliance and trust

Trust signal

Compliance2 records

Lungpacer Medical financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Lungpacer Medical leadership team

Management profile

Number of profiles

Profiles12 records

Lungpacer Medical subsidiaries and ownership

Company hierarchy

Subsidiaries1 record

Lungpacer Medical funding detail

Funding detail

Funding overview

Funding rounds10 records

Investors4 records

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Lungpacer Medical M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Lungpacer Medical

What does Lungpacer Medical do?

Lungpacer Medical develops and sells the AeroPace Neurostimulation System, an FDA-approved temporary transvenous diaphragm neurostimulation (TTDN) device that stimulates the phrenic nerves via a catheter-based approach to activate and strengthen the diaphragm in adult patients on prolonged mechanical ventilation (≥96 hours) who have failed to wean. The system comprises three components (airway pressure sensor, touchscreen neurostimulation console, and temporary transvenous catheter with 30 electrodes) that integrate into existing ICU workflows without surgical implantation. The company is also developing next-generation AeroNova and SupAira systems extending the platform to earlier-stage ventilation and organ donor management.

Is Lungpacer Medical a public or private company?

Lungpacer Medical is a private company. It is classified as venture growth investor backed and is currently operating.

When was Lungpacer Medical founded?

Lungpacer Medical was founded in 2009. It employs 51 to 100 people.

Where is Lungpacer Medical based?

Lungpacer Medical is headquartered in Vancouver, Canada, in the North America region.

How does Lungpacer Medical make money?

Two revenue lines are on record. AeroPace Neurostimulation System (Hardware + Procedure) is the primary driver. The others are professional Services and Clinical Support.

Who are Lungpacer Medical's main competitors?

Emerging players on record are TransMedics and Inspire Medical Systems. Direct peers are Synapse Biomedical and Avery Biomedical Devices. Broad incumbents are Medtronic, Getinge, Dräger, Hamilton Medical, Vyaire Medical and Philips Respironics.

Does Lungpacer Medical have an API?

No public API is recorded for Lungpacer Medical.

What industry is Lungpacer Medical in?

Lungpacer Medical's product category is Respiratory / Critical Care Medical Devices. Its primary akta.pro industry code is HLAHADAJ, Anesthesia & Airway Management Equipment (Workstations, Laryngoscopy, Ventilation adjuncts), with a secondary code of HLAHAGAC, Ventilators & Mechanical Ventilation Systems (ICU/Transport/Home). Its NAICS code is 339112 and its SIC code is 3845.

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Live signals
Financial PostLungpacer Medical Nominated for 2026 Prix Galien USA Award for Best Medical TechnologyLungpacer Medical announced that its AeroPace System has been nominated for the 2026 Prix Galien USA Award for Best Medical Technology. The nomination recognizes the company's FDA-approved diaphragm neurostimulation therapy, which was developed in partnership with Simon Fraser University to help critically ill patients wean off mechanical ventilation. This recognition highlights the commercial launch of the technology at leading U.S. hospitals following its regulatory approval in December 2024.GlobeNewswireLungpacer Announces Health Economic Analysis Demonstrating Clinical and Cost Benefits of AeroPace in Mechanically Ventilated PatientsLungpacer Medical announced a health economic analysis of its AeroPace system, projecting ~$12,000 in average cost savings per patient and ~$12,000 in reduced downstream long-term care costs. The analysis is based on the RESCUE-3 trial and U.S. claims data, with CMS granting a New Technology Add-On Payment of up to $23,650 per case.GlobeNewswireLungpacer Announces Health Economic Analysis Demonstrating Clinical and Cost Benefits of AeroPace in Mechanically Ventilated PatientsLungpacer Medical announced results from a health economic analysis published in Critical Care Medicine, demonstrating that its AeroPace System delivers clinical benefits and significant cost savings for hospitals treating mechanically ventilated patients. The analysis, based on data from the RESCUE-3 randomized controlled trial and U.S. national claims datasets, found reductions in mechanical ventilation duration of 2.8–3.2 days, a greater than 10% improvement in weaning success, and estimated average cost savings of approximately $12,000 per patient during acute care plus an additional $12,000 in reduced downstream long-term care costs. The Centers for Medicare & Medicaid Services granted a New Technology Add-On Payment for AeroPace effective October 1, 2025, and new AMA Category III CPT codes took effect July 1, 2026.American City Business JournalsLungpacer Medical's AeroPace system deployed at Temple HospitalLungpacer Medical's AeroPace system has been deployed at Temple Hospital in Philadelphia, marking a commercial deployment of the medical device at a major regional healthcare facility.American City Business JournalsLungpacer Medical's AeroPace system deployed at Temple HospitalLungpacer Medical's AeroPace system has been deployed at Temple Hospital. The company intends to raise an additional $75 million later this year to expand its sales force and develop a second product.MassDeviceLungpacer picks up reimbursement win for AeroPaceLungpacer Medical announced that the American Medical Association has granted Category III CPT codes for its AeroPace diaphragm neurostimulation system, effective July 1, 2026, enabling standardized reporting of procedures and supporting reimbursement pathway development. The new codes build on the New Technology Add-On Payment from CMS, effective October 1, 2025, which provides up to approximately $23,650 in additional reimbursement per case. The company received FDA premarket approval for AeroPace in late 2024 and reported its first commercial procedure in December 2025, with a next-generation version called AeroNova currently under clinical trial evaluation.GlobeNewswireLungpacer Announces New Category III CPT® Codes for AeroPace® Diaphragm Neurostimulation TherapyLungpacer Medical announced new Category III CPT codes for its AeroPace diaphragm neurostimulation therapy, effective July 1, 2026. The codes build on a CMS New Technology Add-On Payment granting up to $23,650 per case. The company says the codes support broader access for patients needing prolonged mechanical ventilation.BioSpaceLungpacer Medical Announces Presentation of DONATE Data Reporting an Increase in Availability of Donor LungsLungpacer Medical presented DONATE data at the American Transplant Congress 2026, showing transvenous phrenic nerve stimulation increased transplantable lungs from 51.1% to 33.7% of donors. The lung observed-to-expected ratio reached 1.44, 44% more than expected, versus 1.10 in controls.Financial PostLungpacer Medical Announces Presentation of DONATE Data Reporting an Increase in Availability of Donor LungsLungpacer Medical announced results from the DONATE study at the American Transplant Congress 2026 in Boston, showing that temporary transvenous phrenic nerve stimulation using its SupAira system improved oxygenation and reduced atelectasis in 50 brain-dead organ donors. The technology increased the percentage of donors whose lungs were transplanted to 51.1% compared to 33.7% in matched controls, with the observed-to-expected ratio reaching 1.44 versus 1.10 in controls. The findings address a significant gap in transplant medicine, as only about one in five donor lungs are typically recovered, contributing to roughly 20% waitlist mortality.GlobeNewswireLungpacer Medical Announces Presentation of DONATE Data Reporting an Increase in Availability of Donor LungsLungpacer Medical presented DONATE study data at ATC 2026, showing transvenous phrenic nerve stimulation increased transplantable lungs from 33.7% to 51.1% of donors. The lung O:E ratio reached 1.44, 44% more than expected, addressing atelectasis that limits donor lung use.