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LungLife AI

Full company profile

uuid0002eme

Namestring
LungLife AI
Legal namestring
LungLife AI, Inc.
Websiteurl
lunglifeai.com
Company typeenum
Private
Founded yearint
2009
Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersThousand Oaks, United States
HQ citystring
Thousand Oaks
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices3 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
liquid biopsy diagnostics, lung cancer detection, indeterminate lung nodules, circulating tumor cells, clinical laboratory testing
Industry3 codes
1Liquid Biopsy & Minimal Residual Disease (MRD) Precision Testing
CodeHLAAANAGPrimaryYes
2Laboratory Developed Tests (LDTs) & Specialized Clinical Lab Assays
CodeHLAAALANPrimaryNo
3Lung Cancer Screening & Pulmonary Nodule Clinic
CodeHLAKANAIPrimaryNo
NAICS code2 codes
  • Medical Laboratories621511
  • In-Vitro Diagnostic Substance Manufacturing325413
SIC code2 codes
  • Services-Medical Laboratories8071
  • In Vitro & In Vivo Diagnostic Substances2835
Product category
Molecular Diagnostics / Liquid Biopsy
GTM motion3 records

Each record includes

Type, Description, Source

Revenue model3 records
1Laboratory Diagnostic Testing Services
TypeOne Time License
Description

LungLB test performed in CLIA-certified laboratory as a Laboratory Developed Test (LDT). Revenue generated from test fees per patient sample. Medicare price established at $2,030 per test.

lunglifeai.com
2Licensing and Royalty Revenue
TypeLicensing Royalties
Description

Following exclusive license and distribution agreement with Circulogene, LungLife receives royalty payments of 20% of net revenue (first year) and 15% thereafter, plus guaranteed minimum royalty payments of $450,000 for first three quarters. Advanced payment of $375,000 received at signing.

lunglifeai.com
3SEC Filing - Exempt Securities Offering
TypeOne Time License
Description

Form D notice filed for exempt securities offering worth $315,780.

sec.gov
Marketing channels6 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels3 records

Each record includes

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

Cost components4 values
Personnel, Technology or R&D, Operations, Marketing or Sales
Pricing details2 tiers
1LungLB Test - Standard Pricing
ModelUnit PricingBilling cadencePay-as-you-go
Notes

$2,030 per test as established by Centers for Medicare & Medicaid Services (CMS) effective January 1, 2023

lunglifeai.com
2Licensing Royalty Structure
ModelTransaction based/ take rateBilling cadencePay-as-you-go
Notes

20% of net revenue first year, reducing to 15% thereafter. Guaranteed minimum royalty payments of $450,000 for first three quarters. Asset Purchase Option of $6,200,000 less payments received.

lunglifeai.com
GTM typeB2B
B2B
Offering typeServices
Services
Brand1 of 2 records shown
1LungLB
Description

A blood-based diagnostic test for early detection of lung cancer using liquid biopsy technology with AI-enhanced analysis. The test is designed to provide clinicians additional information for evaluating indeterminate lung nodules.

lunglifeai.com
+1 more record
Core offering1 text field

LungLife AI develops and performs the LungLB® test, a blood-based liquid biopsy that uses rare-cell enrichment combined with FISH-based detection of circulating genetically abnormal cells and AI-enhanced 3D image analysis to classify patients with indeterminate lung nodules as low or high risk for lung cancer. The test is run as a Laboratory Developed Test (LDT) in the company's CLIA-certified, CAP-accredited, NYSDOH-CLEP-permitted laboratory in Thousand Oaks, California, and is targeted at pulmonologists, thoracic physicians, and hospital-based nodule clinics.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 4 values shown
  • 81% positive predictive value (PPV) in small nodules (<15mm), compared to ~60% PPV for standard care and 67% PPV for PET scan
+3 more records
Product overview1 text field

LungLife AI offers a single unified product: the LungLB test, a liquid biopsy diagnostic solution for early lung cancer detection. The test uses a minimally invasive blood draw combined with AI-enhanced rare-cell enrichment technology and FISH (fluorescent in-situ hybridization) protocol to identify circulating genetically abnormal cells. It is performed in the company's CLIA-certified laboratory in Thousand Oaks, California, and is designed to provide clinicians with additional information to evaluate indeterminate lung nodules following CT scans.

Product and service1 record
1LungLB Test
CategoryMolecular Diagnostics / Liquid Biopsy
Description

A blood-based liquid biopsy diagnostic test that uses rare-cell enrichment combined with FISH (fluorescent in-situ hybridization) probes and AI-enhanced 3D image acquisition to identify circulating genetically abnormal cells from a peripheral blood sample. Classifies patients with indeterminate pulmonary nodules as low or high risk for lung cancer. Performed as a Laboratory Developed Test (LDT) in LungLife's CLIA-certified, CAP-accredited laboratory in Thousand Oaks, California. Targeted at pulmonologists, thoracic oncologists, and hospital-based nodule clinics managing the ~1.5 million indeterminate lung nodules identified annually in the US.

Scale indicator11 records

Each record includes

Type, Value, Description, Source

Partnership1 partner
Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2025-04-17
Description

Exclusive license and distribution agreement for commercial distribution of LungLB test in the US. Circulogene receives exclusive rights to improve, develop, market, distribute, and sell the test. LungLife receives advanced payment of $375,000, further $375,000 at completion, plus 20% royalties (reducing to 15% after year 1) with guaranteed minimum $450,000. Circulogene has option to purchase IP for $6.2M less payments received.

Recent move10 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Biodesix offers the Nodify Lung blood-based diagnostic tests (Nodify XL2 and Nodify CDT) for evaluating indeterminate pulmonary nodules, directly competing with LungLB in the same clinician use case and patient segment.

TypeDirect peer
Description

Veracyte's Percepta Genomic Sequencing Classifier uses a bronchoscopy sample to assess lung cancer risk in suspicious nodules; both companies address the indeterminate pulmonary nodule diagnostic decision point for pulmonologists.

3Oncocyte (now Insight Molecular Diagnostics)
TypeDirect peer
Description

Oncocyte's DetermaRx is a molecular test for early-stage lung cancer risk stratification, targeting the same pulmonologist/thoracic oncologist customer base with a tissue- or blood-based genomic assay.

TypeDirect peer
Description

EarlyCDT-Lung is a blood-based autoantibody test for early lung cancer detection; competes head-to-head with LungLB as a non-invasive blood draw for at-risk patients.

TypeBroad incumbent
Description

Guardant360 and Guardant Shield are established liquid biopsy tests for oncology; while broader in scope, Guardant is a major player that could extend into lung nodule management, posing an indirect threat to LungLB.

TypeBroad incumbent
Description

Exact Sciences is the commercial leader in non-invasive cancer screening (Cologuard); its scale, salesforce and pipeline ambitions represent the kind of large incumbent LungLB would compete against for guideline inclusion and payor coverage.

TypeBroad incumbent
Description

Natera offers Signatera (tumor-informed MRD) and other blood-based oncology tests; an established liquid biopsy operator with broad commercial reach and significant R&D capabilities relevant to the lung cancer space.

TypeBroad incumbent
Description

NeoGenomics operates a major oncology-focused clinical lab network and offers a menu of molecular and liquid biopsy services, including for lung cancer, comparable in lab-based diagnostic model to LungLife.

TypeBroad incumbent
Description

Resolution Bioscience (now part of Agilent) developed a cfDNA-based liquid biopsy for NSCLC; comparable technology category (blood-based cancer mutation detection) and similar clinical-use positioning as LungLB.

TypeEmerging player
Description

Circulogene is LungLife AI's exclusive US distribution partner and operates its own CLIA lab; strategically aligned commercially and operates a comparable liquid-biopsy lab services model.

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 highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers4 records

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 capability5 records

Each record includes

Type, Description, Source

AI maturity
App detail

Has app

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles1 record

Each record includes

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

No data
Compliance4 records

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds13 records

Each record includes

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

Investors3 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 →

LungLife AI

Molecular Diagnostics / Liquid Biopsylunglifeai.com

LungLife AI firmographics

Firmographics
Name
LungLife AI
Legal name
LungLife AI, Inc.
Website
https://lunglifeai.com
Company type
Private
Founded year
2009
Operating status
Operating
Headcount range
11–50 employees
Ownership category
akta.pro rank

LungLife AI industry classification

Industry
Product category
Molecular Diagnostics / Liquid Biopsy
NAICS
Medical Laboratories (621511), In-Vitro Diagnostic Substance Manufacturing (325413)
SIC
Services-Medical Laboratories (8071), In Vitro & In Vivo Diagnostic Substances (2835)
akta.pro primary industry
Liquid Biopsy & Minimal Residual Disease (MRD) Precision Testing (HLAAANAG)
akta.pro secondary industries
Laboratory Developed Tests (LDTs) & Specialized Clinical Lab Assays (HLAAALAN), Lung Cancer Screening & Pulmonary Nodule Clinic (HLAKANAI)

Keywords

  • Liquid biopsy diagnostics
  • Lung cancer detection
  • Indeterminate lung nodules
  • Circulating tumor cells
  • Clinical laboratory testing

Where LungLife AI is headquartered

Location

Headquarters

HQ city
Thousand Oaks
HQ country
United States
HQ region
North America

Offices3 records

Markets served

LungLife AI business model

Business model
GTM type
B2B
Offering type
Services
Cost components
Personnel, Technology or R&D, Operations, Marketing or Sales

Revenue model

  1. Laboratory Diagnostic Testing Services: LungLB test performed in CLIA-certified laboratory as a Laboratory Developed Test (LDT). Revenue generated from test fees per patient sample. Medicare price established at $2,030 per test.
  2. Licensing and Royalty Revenue: Following exclusive license and distribution agreement with Circulogene, LungLife receives royalty payments of 20% of net revenue (first year) and 15% thereafter, plus guaranteed minimum royalty payments of $450,000 for first three quarters. Advanced payment of $375,000 received at signing.
  3. SEC Filing - Exempt Securities Offering: Form D notice filed for exempt securities offering worth $315,780.

Pricing tiers

ModelBillingPrice
Unit PricingPay-as-you-goLungLB Test - Standard Pricing
Transaction based/ take ratePay-as-you-goLicensing Royalty Structure

Go-to-market motion3 records

Distribution channels3 records

Marketing channels6 records

LungLife AI product offering

Product offering

Core offering

LungLife AI develops and performs the LungLB® test, a blood-based liquid biopsy that uses rare-cell enrichment combined with FISH-based detection of circulating genetically abnormal cells and AI-enhanced 3D image analysis to classify patients with indeterminate lung nodules as low or high risk for lung cancer. The test is run as a Laboratory Developed Test (LDT) in the company's CLIA-certified, CAP-accredited, NYSDOH-CLEP-permitted laboratory in Thousand Oaks, California, and is targeted at pulmonologists, thoracic physicians, and hospital-based nodule clinics.

Product overview

LungLife AI offers a single unified product: the LungLB test, a liquid biopsy diagnostic solution for early lung cancer detection. The test uses a minimally invasive blood draw combined with AI-enhanced rare-cell enrichment technology and FISH (fluorescent in-situ hybridization) protocol to identify circulating genetically abnormal cells. It is performed in the company's CLIA-certified laboratory in Thousand Oaks, California, and is designed to provide clinicians with additional information to evaluate indeterminate lung nodules following CT scans.

Differentiator

Problem solved

Functional benefit

Brands

  • LungLB: A blood-based diagnostic test for early detection of lung cancer using liquid biopsy technology with AI-enhanced analysis. The test is designed to provide clinicians additional information for evaluating indeterminate lung nodules.
  • LiquidBiopsy

Products and services

  • LungLB Test A blood-based liquid biopsy diagnostic test that uses rare-cell enrichment combined with FISH (fluorescent in-situ hybridization) probes and AI-enhanced 3D image acquisition to identify circulating genetically abnormal cells from a peripheral blood sample. Classifies patients with indeterminate pulmonary nodules as low or high risk for lung cancer. Performed as a Laboratory Developed Test (LDT) in LungLife's CLIA-certified, CAP-accredited laboratory in Thousand Oaks, California. Targeted at pulmonologists, thoracic oncologists, and hospital-based nodule clinics managing the ~1.5 million indeterminate lung nodules identified annually in the US.

Quantifiable outcome

  • 81% positive predictive value (PPV) in small nodules (<15mm), compared to ~60% PPV for standard care and 67% PPV for PET scan
  • +3 more outcomes

Companies that use LungLife AI

Customer profile

Named customers4 records

Segments3 records

Ideal customer profiles2 records

LungLife AI technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

AI capability5 records

Feature3 records

LungLife AI partnerships and signals

Strategic signal

Partnerships

One partnership is on record.

  • Circulogene Theranostics, Inc.coreChannel Partner/ Reseller/ Distributor · 17 April 2025Exclusive license and distribution agreement for commercial distribution of LungLB test in the US. Circulogene receives exclusive rights to improve, develop, market, distribute, and sell the test. LungLife receives advanced payment of $375,000, further $375,000 at completion, plus 20% royalties (reducing to 15% after year 1) with guaranteed minimum $450,000. Circulogene has option to purchase IP for $6.2M less payments received.

Scale indicators11 records

Recent moves10 records

Expansion highlights5 records

LungLife AI competitors and assessment

Company assessment

Direct peers

  • Biodesix: Biodesix offers the Nodify Lung blood-based diagnostic tests (Nodify XL2 and Nodify CDT) for evaluating indeterminate pulmonary nodules, directly competing with LungLB in the same clinician use case and patient segment.
  • Veracyte: Veracyte's Percepta Genomic Sequencing Classifier uses a bronchoscopy sample to assess lung cancer risk in suspicious nodules; both companies address the indeterminate pulmonary nodule diagnostic decision point for pulmonologists.
  • Oncocyte (now Insight Molecular Diagnostics): Oncocyte's DetermaRx is a molecular test for early-stage lung cancer risk stratification, targeting the same pulmonologist/thoracic oncologist customer base with a tissue- or blood-based genomic assay.
  • Oncimmune (now Biodesix, brand EarlyCDT-Lung): EarlyCDT-Lung is a blood-based autoantibody test for early lung cancer detection; competes head-to-head with LungLB as a non-invasive blood draw for at-risk patients.

Broad incumbents

  • Guardant Health: Guardant360 and Guardant Shield are established liquid biopsy tests for oncology; while broader in scope, Guardant is a major player that could extend into lung nodule management, posing an indirect threat to LungLB.
  • Exact Sciences: Exact Sciences is the commercial leader in non-invasive cancer screening (Cologuard); its scale, salesforce and pipeline ambitions represent the kind of large incumbent LungLB would compete against for guideline inclusion and payor coverage.
  • Natera: Natera offers Signatera (tumor-informed MRD) and other blood-based oncology tests; an established liquid biopsy operator with broad commercial reach and significant R&D capabilities relevant to the lung cancer space.
  • NeoGenomics: NeoGenomics operates a major oncology-focused clinical lab network and offers a menu of molecular and liquid biopsy services, including for lung cancer, comparable in lab-based diagnostic model to LungLife.
  • Resolution Bioscience (acquired by Agilent): Resolution Bioscience (now part of Agilent) developed a cfDNA-based liquid biopsy for NSCLC; comparable technology category (blood-based cancer mutation detection) and similar clinical-use positioning as LungLB.

Emerging players

  • Circulogene Theranostics: Circulogene is LungLife AI's exclusive US distribution partner and operates its own CLIA lab; strategically aligned commercially and operates a comparable liquid-biopsy lab services model.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat5 records

Key risks6 records

Key highlights6 records

Customer concentration

LungLife AI social profiles

Digital presence

LungLife AI compliance and trust

Trust signal

Compliance4 records

LungLife AI financial estimates

Financial estimate

Revenue estimate

Valuation estimate

LungLife AI leadership team

Management profile

Number of profiles

Profiles1 record

LungLife AI funding detail

Funding detail

Funding overview

Funding rounds13 records

Investors3 records

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

LungLife AI 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 LungLife AI

What does LungLife AI do?

LungLife AI develops and performs the LungLB® test, a blood-based liquid biopsy that uses rare-cell enrichment combined with FISH-based detection of circulating genetically abnormal cells and AI-enhanced 3D image analysis to classify patients with indeterminate lung nodules as low or high risk for lung cancer. The test is run as a Laboratory Developed Test (LDT) in the company's CLIA-certified, CAP-accredited, NYSDOH-CLEP-permitted laboratory in Thousand Oaks, California, and is targeted at pulmonologists, thoracic physicians, and hospital-based nodule clinics.

Is LungLife AI a public or private company?

LungLife AI is a private company. It is classified as unknown and is currently operating.

When was LungLife AI founded?

LungLife AI was founded in 2009. It employs 11 to 50 people.

Where is LungLife AI based?

LungLife AI is headquartered in Thousand Oaks, United States, in the North America region.

How does LungLife AI make money?

Three revenue lines are on record. Laboratory Diagnostic Testing Services are the primary driver. The others are licensing and Royalty Revenue and SEC Filing - Exempt Securities Offering.

Who are LungLife AI's main competitors?

Direct peers on record are Biodesix, Veracyte, Oncocyte (now Insight Molecular Diagnostics) and Oncimmune (now Biodesix, brand EarlyCDT-Lung). Broad incumbents are Guardant Health, Exact Sciences, Natera, NeoGenomics and Resolution Bioscience (acquired by Agilent). Circulogene Theranostics is listed as an emerging player.

Does LungLife AI have an API?

No public API is recorded for LungLife AI.

What industry is LungLife AI in?

LungLife AI's product category is Molecular Diagnostics / Liquid Biopsy. Its primary akta.pro industry code is HLAAANAG, Liquid Biopsy & Minimal Residual Disease (MRD) Precision Testing, with a secondary code of HLAAALAN, Laboratory Developed Tests (LDTs) & Specialized Clinical Lab Assays. Its NAICS code is 621511 and its SIC code is 8071.

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