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Cepheid

Full company profile

uuid0002v5p

Namestring
Cepheid
Legal namestring
Cepheid
Websiteurl
cepheid.com
Company typeenum
Private
Founded yearint
1996
Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
5,001–10,000
akta.pro rankint
HeadquartersSunnyvale, United States
HQ citystring
Sunnyvale
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
molecular diagnostics, PCR testing systems, infectious disease detection, point-of-care diagnostics, cartridge-based testing
Industry3 codes
1Molecular Diagnostics (PCR/NAAT/NGS-based IVD)
CodeHLAHAAADPrimaryYes
2Molecular Diagnostics (PCR/qPCR, NGS-based assays)
CodeHLAAALAAPrimaryNo
3Multiplex & High-Throughput Diagnostics Platforms (microarrays, digital PCR, lab automation-enabled assays)
CodeHLAAALALPrimaryNo
NAICS code2 codes
  • Medical Equipment and Supplies Manufacturing3391
  • Surgical and Medical Instrument Manufacturing339112
SIC code2 codes
  • In Vitro & In Vivo Diagnostic Substances2835
  • Surgical & Medical Instruments & Apparatus3841
Product category
Molecular Diagnostics
GTM motion3 records

Each record includes

Type, Description, Source

Revenue model2 records
1Molecular Diagnostics Instruments
TypeHardware Sales
Description

Cepheid generates revenue through the sale of GeneXpert instruments and systems to healthcare facilities and laboratories

pitchgrade.com
2Diagnostic Test Reagents and Cartridges
TypeSubscription Recurring
Description

Recurring revenue from the sale of Xpert test cartridges and reagents that run on the GeneXpert platform. This creates recurring consumables revenue tied to the installed base

pitchgrade.com
Marketing channels5 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels3 records

Each record includes

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

Cost components6 values
Supply Chain, Technology or R&D, Personnel, Operations, Marketing or Sales, Infrastructure
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 2 records shown
1GeneXpert
Description

Cepheid's flagship molecular diagnostic testing system platform.

cepheid.com
+1 more record
Core offering1 text field

Cepheid develops, manufactures, and sells the GeneXpert family of automated real-time PCR molecular diagnostic instruments (GeneXpert System, GeneXpert Infinity, GeneXpert Xpress) and a broad menu of single-use Xpert test cartridges for respiratory infections, hospital-acquired infections, tuberculosis and emerging infectious diseases, blood virology/women's health/sexual health, and oncology/human genetics. Results are typically delivered in about one hour from specimen to answer, supported by GeneXpert Dx Software, GeneXpert Xpertise Software, and Cepheid C360 connectivity solutions.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 4 values shown
  • Xpert GI Panel provides results in approximately 74 minutes compared to 48-72 hours for traditional culture methods
+3 more records
Product overview1 text field

Cepheid is a molecular diagnostics company offering a unified platform-plus-tests architecture centered on the GeneXpert System. The GeneXpert family of instruments (GeneXpert System, GeneXpert Infinity, GeneXpert Xpress) provides a flexible, fully scalable molecular diagnostics platform with cartridge-based automated sample processing and real-time PCR. The portfolio includes multiple diagnostic test categories: Respiratory tests (including Xpert Xpress CoV-2/Flu/RSV plus, Xpert Xpress Flu/RSV, Xpert Xpress Flu, Xpert Xpress Strep A), HAI & Infectious Disease tests (including Xpert GI Panel, Xpert SA Nasal Complete, Xpert MRSA/SA SSTI, Xpert C. difficile/Epi, Xpert Norovirus, Xpert Carba-R, Xpert vanA), Blood Virology/Women's Health/Sexual Health tests (including Xpert HCV, Xpert CT/NG, Xpert GBS LB XC, Xpert TV, Xpert Xpress GBS), TB & Emerging Infectious Diseases tests (including Xpert MTB/RIF, Xpert MTB/XDR, Xpert Mpox, Xpert Hemorrhagic Fever Panel), and Oncology & Human Genetics tests (including Xpert BCR-ABL Ultra, Xpert FII & FV, Xpert NPM1 Mutation RUO, Xpert PML RARA RUO). The offering is complemented by GeneXpert Dx Software and GeneXpert Xpertise Software for instrument management and data handling, and Cepheid C360 for connectivity solutions.

Product and service31 records
1GeneXpert System
CategoryMolecular diagnostics instrument system
Description

Fully scalable cartridge-based molecular diagnostics platform that automates sample processing and real-time PCR testing, providing a broad test menu for any setting from core lab to near-patient applications. Used by hospitals, clinical laboratories, and public health programs.

2GeneXpert Infinity System
CategoryMolecular diagnostics instrument system
Description

High-throughput version of the GeneXpert platform designed for larger laboratory settings requiring higher testing volumes. Used by clinical laboratories and high-volume hospital labs.

3GeneXpert Xpress
CategoryMolecular diagnostics instrument system (point-of-care)
Description

Point-of-care variant of the GeneXpert system designed for rapid testing in near-patient settings such as physician offices and urgent care clinics.

4GeneXpert Dx Software
CategoryInstrument management software
Description

Diagnostic software for the GeneXpert system that manages test processing, results display, and quality control. Used by laboratories and hospitals running GeneXpert instruments.

5GeneXpert Xpertise Software
CategoryEnterprise laboratory software
Description

Enterprise software platform for GeneXpert systems providing connectivity, data management, and workflow optimization across the installed base. Used by multi-site hospital networks and reference laboratories.

6Cepheid C360
CategoryConnectivity and integration software
Description

Connectivity solution enabling integration between GeneXpert systems and laboratory information systems. Used by hospital IT and laboratory informatics teams.

7Xpert GI Panel
CategoryMolecular diagnostic test cartridge (HAI/gastrointestinal)
Description

FDA-cleared and CE-marked under IVDR multiplex PCR assay detecting 11 bacterial, viral, and parasitic gastrointestinal pathogens from a single stool specimen in approximately 74 minutes. Used by hospitals and clinical laboratories for infectious gastroenteritis testing.

8Xpert MTB/RIF
CategoryMolecular diagnostic test cartridge (TB)
Description

WHO-prequalified molecular test for tuberculosis detection that also identifies rifampicin resistance, providing results in approximately 90 minutes. Used by TB programs, hospitals, and public health laboratories globally.

9Xpert Xpress MVP (Mpox)
CategoryMolecular diagnostic test cartridge (emerging infectious disease)
Description

Molecular test for mpox (Monkeypox) virus detection. Used by public health laboratories and clinical labs responding to mpox outbreaks.

10Xpert Xpress CoV-2/Flu/RSV plus
CategoryMolecular diagnostic test cartridge (respiratory)
Description

Multiplex respiratory panel detecting SARS-CoV-2, influenza A/B, and RSV from a single sample with rapid turnaround. Used by hospitals, urgent care, and physician offices.

11Xpert Xpress Flu/RSV
CategoryMolecular diagnostic test cartridge (respiratory)
Description

Rapid multiplex test for influenza A, influenza B, and RSV detection. Used by physician offices, urgent care, and hospital labs.

12Xpert Xpress Flu
CategoryMolecular diagnostic test cartridge (respiratory, point-of-care)
Description

Rapid point-of-care test for influenza A and B. Used in physician offices, urgent care, and hospital point-of-care settings.

13Xpert Xpress Strep A
CategoryMolecular diagnostic test cartridge (respiratory, point-of-care)
Description

Rapid test for Group A Streptococcus detection from throat swab specimens. Used by physician offices, urgent care, and hospital point-of-care settings.

14Xpert Xpress CoV-2 plus
CategoryMolecular diagnostic test cartridge (respiratory, point-of-care)
Description

Rapid point-of-care PCR test for SARS-CoV-2 detection. Used by hospitals, urgent care, and physician offices.

15Xpert SA Nasal Complete
CategoryMolecular diagnostic test cartridge (HAI)
Description

Test for Staphylococcus aureus and methicillin-resistant S. aureus (MRSA) screening from nasal specimens. Used by hospitals for pre-surgical and infection control screening.

16Xpert MRSA/SA SSTI
CategoryMolecular diagnostic test cartridge (HAI)
Description

Test for MRSA and S. aureus detection from skin and soft tissue infections. Used by hospital infection control and emergency settings.

17Xpert MRSA/SA Blood Culture
CategoryMolecular diagnostic test cartridge (HAI/bloodstream)
Description

Test for MRSA and S. aureus detection directly from positive blood cultures. Used by hospital microbiology laboratories for bloodstream infection workups.

18Xpert MRSA NxG
CategoryMolecular diagnostic test cartridge (HAI)
Description

Next-generation MRSA screening test with enhanced performance characteristics. Used by hospitals for active surveillance and infection prevention.

19Xpert C. difficile/Epi
CategoryMolecular diagnostic test cartridge (HAI)
Description

Test for Clostridioides difficile detection and ribotyping to identify epidemic strains. Used by hospitals and stewardship/infection control programs.

20Xpert Norovirus
CategoryMolecular diagnostic test cartridge (HAI/gastrointestinal)
Description

Rapid molecular test for norovirus detection. Used by hospital laboratories during norovirus outbreaks.

21Xpert vanA
CategoryMolecular diagnostic test cartridge (HAI/drug resistance)
Description

Test for vancomycin resistance gene (vanA) detection to identify Vancomycin-resistant Enterococcus (VRE). Used by hospital infection control and stewardship programs.

22Xpert Carba-R
CategoryMolecular diagnostic test cartridge (HAI/drug resistance)
Description

Test for carbapenem resistance genes detection, supporting CPE screening programs. Used by hospital infection prevention and antimicrobial stewardship teams.

23Xpert HCV
CategoryMolecular diagnostic test cartridge (blood virology, point-of-care)
Description

FDA-authorized test using a 100 µL fingerstick blood sample for Hepatitis C virus detection at point of care. Used by public health programs, point-of-care settings, and outreach screening.

24Xpert CT/NG
CategoryMolecular diagnostic test cartridge (sexual health)
Description

Test for Chlamydia trachomatis and Neisseria gonorrhoeae detection. Used by sexual health clinics, hospitals, and reference laboratories.

25Xpert GBS LB XC
CategoryMolecular diagnostic test cartridge (women's health)
Description

Test for Group B Streptococcus detection from Lim broth enriched samples for prenatal screening. Used by hospital labor and delivery and prenatal clinics.

26Xpert Xpress GBS
CategoryMolecular diagnostic test cartridge (women's health, point-of-care)
Description

Rapid test for Group B Streptococcus detection. Used by hospital labor and delivery and prenatal point-of-care settings.

27Xpert TV
CategoryMolecular diagnostic test cartridge (sexual health)
Description

Test for Trichomonas vaginalis detection. Used by sexual health clinics, women's health providers, and clinical laboratories.

28Xpert BCR-ABL Ultra
CategoryMolecular diagnostic test cartridge (oncology)
Description

Quantitative test for BCR-ABL fusion transcript monitoring in chronic myeloid leukemia (CML) patients. Used by hospital hematology/oncology labs and reference laboratories.

29Xpert FII & FV
CategoryMolecular diagnostic test cartridge (human genetics)
Description

Test for Factor II and Factor V Leiden mutations associated with thrombophilia. Used by clinical laboratories supporting hematology and prenatal genetics workflows.

30Xpert Hemorrhagic Fever Panel
CategoryMolecular diagnostic test cartridge (emerging infectious disease)
Description

Rapid molecular test detecting Ebola virus (including Bundibugyo strain), Crimean Congo hemorrhagic fever, Marburg, and Lassa viruses with results in approximately one hour. Used by public health agencies, ministries of health, and outbreak response teams.

31Xpert MTB/XDR
CategoryMolecular diagnostic test cartridge (TB/drug resistance)
Description

WHO-prequalified test detecting resistance to multiple TB drugs including isoniazid, ethionamide, fluoroquinolones, and second-line injectables, with results in about 90 minutes. Used by national TB programs and reference laboratories in high-burden settings.

Scale indicator3 records

Each record includes

Type, Value, Description, Source

Partnership7 partners
Strategic tierMajorTypeGTM or Marketing PartnerAnnounced on2026-06-12
Description

Cepheid coordinated with the U.S. government to support diagnostic response to the Ebola Bundibugyo outbreak in DRC and Uganda, following WHO's declaration as a Public Health Emergency of International Concern.

Strategic tierMajorTypeGTM or Marketing PartnerAnnounced on2026-06-12
Description

Cepheid coordinated with WHO to accelerate deployment and expand testing capacity for Ebola Bundibugyo outbreak response following the WHO's declaration of the outbreak as a Public Health Emergency of International Concern.

Strategic tierMajorTypeGTM or Marketing PartnerAnnounced on2026-06-12
Description

Cepheid coordinated with Africa CDC to accelerate deployment and expand testing capacity for Ebola Bundibugyo outbreak response across affected regions.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-06-11
Description

The Fleming Initiative (a partnership between Imperial College London and Imperial College Healthcare NHS Trust) and Cepheid launched the TRACE-CPE study, a two-and-a-half-year research project evaluating rapid molecular screening for carbapenemase-producing Enterobacterales (CPE) drug-resistant bacteria in NHS hospitals. The study compares one-hour rapid diagnostics against standard 48-hour culture-based methods to assess clinical, infection control, and cost impacts.

5U.S. CDC
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-02-18
Description

Cepheid was selected by the U.S. CDC as one of four national collaborators under a federal IDIQ contract to accelerate development and deployment of rapid diagnostic technologies during public health emergencies. The collaboration grants Cepheid early access to outbreak samples, genomic sequences, and critical reference materials to accelerate next-generation diagnostic assay creation. The partnership builds on Cepheid's track record including the launch of the first point-of-care PCR test for SARS-CoV-2 in the United States.

biospace.com
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-05-01
Description

Cepheid and Oxford Nanopore Technologies have expanded their partnership to phase two, building on successful phase one collaboration that produced a beta workflow for bacterial and fungal pathogen profiling in sepsis and bloodstream infection research. The updated workflow enables pathogen identification, antimicrobial resistance profiling, and genomic antibiotic susceptibility testing predictions, with a co-commercialized RUO launch planned for Q3-2026. Both companies share a long-term ambition to deliver an end-to-end in vitro diagnostic solution for complex infectious diseases.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2021-12-16
Description

Cepheid acquired OncoMark Ltd., a UCD spin-out company that developed the OncoMasTR test for breast cancer. The test is aimed at reducing unnecessary chemotherapy and will be launched on Cepheid's GeneXpert platform in global markets.

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

Operates the cobas Liat (POC), cobas 6800/8800 (high-throughput), and broader molecular diagnostics menu. Comparable as a broad incumbent with overlapping PCR multiplex and point-of-care molecular capabilities competing for the same hospital and reference-lab customers.

TypeDirect peer
Description

Panther Fusion and Aptima molecular diagnostics franchises compete head-to-head with GeneXpert in women's health, STI, and respiratory testing. Closely aligned business model (instrument + cartridge consumables) and overlapping hospital customer base.

TypeDirect peer
Description

BioFire FilmArray syndromic panels directly compete with Cepheid's multiplex respiratory and GI panels. Same POC-to-lab workflow, similar customer base in hospital microbiology, and comparable regulatory pathway (FDA-cleared cartridge-based multiplex PCR).

TypeBroad incumbent
Description

m-PIMA and ID NOW platforms compete in point-of-care molecular diagnostics, with Abbott leveraging a far broader diagnostics portfolio and global sales reach to pressure Cepheid in both POC and central-lab settings.

TypeDirect peer
Description

QIAstat-Dx is a direct multiplex cartridge-based PCR competitor to GeneXpert, particularly in respiratory and GI testing. Comparable cartridge consumables model, regulatory positioning, and target hospital/urgent-care customer base.

TypeBroad incumbent
Description

BD MAX system and BD Veritor offer molecular and rapid diagnostics that overlap with GeneXpert menu categories. Competes broadly across HAI, women's health, and respiratory testing with a larger installed base of hospital customers.

TypeBroad incumbent
Description

Acquired Luminex and now offers multiplex molecular and immunoassay platforms. Competes in syndromic respiratory testing and broader hospital diagnostics where Cepheid's GeneXpert menu is sold.

TypeEmerging player
Description

Specializes in rapid identification and antimicrobial susceptibility testing (e.g., Pheno system), partially overlapping with Cepheid's Xpert Carba-R and antibiotic stewardship offerings. Smaller and more focused, but addresses the same AMR clinical workflow.

TypeEmerging player
Description

T2 Magnetic Resonance-based direct-from-blood molecular diagnostics for sepsis pathogens. Targets a similar rapid molecular sepsis use case as Cepheid's emerging bloodstream infection workflow with Oxford Nanopore.

TypeOthers
Description

Sequencing platform partner rather than a direct competitor, but a strategic adjacency: a successful Phase 2 co-developed sepsis/BSI workflow could become a future substitute for cartridge-based multiplex PCR, making Nanopore a peer by category as much as by partnership.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses4 records

Each record includes

Headline, Details, Source

Competitive moat6 records

Each record includes

Type, Details

Key risks5 records

Each record includes

Headline, Details, Source

Key highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers5 records

Each record includes

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

Segment4 records

Each record includes

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

Ideal customer profile4 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

Feature7 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles13 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 rounds7 records

Each record includes

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

Investors5 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&A1 record

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 →

Cepheid

Molecular Diagnosticscepheid.com

Cepheid firmographics

Firmographics
Name
Cepheid
Legal name
Cepheid
Website
https://cepheid.com
Company type
Private
Founded year
1996
Operating status
Operating
Headcount range
5,001–10,000 employees
Ownership category
akta.pro rank

Cepheid industry classification

Industry
Product category
Molecular Diagnostics
NAICS
Medical Equipment and Supplies Manufacturing (3391), Surgical and Medical Instrument Manufacturing (339112)
SIC
In Vitro & In Vivo Diagnostic Substances (2835), Surgical & Medical Instruments & Apparatus (3841)
akta.pro primary industry
Molecular Diagnostics (PCR/NAAT/NGS-based IVD) (HLAHAAAD)
akta.pro secondary industries
Molecular Diagnostics (PCR/qPCR, NGS-based assays) (HLAAALAA), Multiplex & High-Throughput Diagnostics Platforms (microarrays, digital PCR, lab automation-enabled assays) (HLAAALAL)

Keywords

  • Molecular diagnostics
  • PCR testing systems
  • Infectious disease detection
  • Point-of-care diagnostics
  • Cartridge-based testing

Where Cepheid is headquartered

Location

Headquarters

HQ city
Sunnyvale
HQ country
United States
HQ region
North America

Offices1 record

Markets served

Cepheid business model

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

Revenue model

  1. Molecular Diagnostics Instruments: Cepheid generates revenue through the sale of GeneXpert instruments and systems to healthcare facilities and laboratories
  2. Diagnostic Test Reagents and Cartridges: Recurring revenue from the sale of Xpert test cartridges and reagents that run on the GeneXpert platform. This creates recurring consumables revenue tied to the installed base

Go-to-market motion3 records

Distribution channels3 records

Marketing channels5 records

Cepheid product offering

Product offering

Core offering

Cepheid develops, manufactures, and sells the GeneXpert family of automated real-time PCR molecular diagnostic instruments (GeneXpert System, GeneXpert Infinity, GeneXpert Xpress) and a broad menu of single-use Xpert test cartridges for respiratory infections, hospital-acquired infections, tuberculosis and emerging infectious diseases, blood virology/women's health/sexual health, and oncology/human genetics. Results are typically delivered in about one hour from specimen to answer, supported by GeneXpert Dx Software, GeneXpert Xpertise Software, and Cepheid C360 connectivity solutions.

Product overview

Cepheid is a molecular diagnostics company offering a unified platform-plus-tests architecture centered on the GeneXpert System. The GeneXpert family of instruments (GeneXpert System, GeneXpert Infinity, GeneXpert Xpress) provides a flexible, fully scalable molecular diagnostics platform with cartridge-based automated sample processing and real-time PCR. The portfolio includes multiple diagnostic test categories: Respiratory tests (including Xpert Xpress CoV-2/Flu/RSV plus, Xpert Xpress Flu/RSV, Xpert Xpress Flu, Xpert Xpress Strep A), HAI & Infectious Disease tests (including Xpert GI Panel, Xpert SA Nasal Complete, Xpert MRSA/SA SSTI, Xpert C. difficile/Epi, Xpert Norovirus, Xpert Carba-R, Xpert vanA), Blood Virology/Women's Health/Sexual Health tests (including Xpert HCV, Xpert CT/NG, Xpert GBS LB XC, Xpert TV, Xpert Xpress GBS), TB & Emerging Infectious Diseases tests (including Xpert MTB/RIF, Xpert MTB/XDR, Xpert Mpox, Xpert Hemorrhagic Fever Panel), and Oncology & Human Genetics tests (including Xpert BCR-ABL Ultra, Xpert FII & FV, Xpert NPM1 Mutation RUO, Xpert PML RARA RUO). The offering is complemented by GeneXpert Dx Software and GeneXpert Xpertise Software for instrument management and data handling, and Cepheid C360 for connectivity solutions.

Differentiator

Problem solved

Functional benefit

Brands

  • GeneXpert: Cepheid's flagship molecular diagnostic testing system platform.
  • Xpert

Products and services

  • GeneXpert System Fully scalable cartridge-based molecular diagnostics platform that automates sample processing and real-time PCR testing, providing a broad test menu for any setting from core lab to near-patient applications. Used by hospitals, clinical laboratories, and public health programs.
  • GeneXpert Infinity System High-throughput version of the GeneXpert platform designed for larger laboratory settings requiring higher testing volumes. Used by clinical laboratories and high-volume hospital labs.
  • GeneXpert Xpress Point-of-care variant of the GeneXpert system designed for rapid testing in near-patient settings such as physician offices and urgent care clinics.
  • GeneXpert Dx Software Diagnostic software for the GeneXpert system that manages test processing, results display, and quality control. Used by laboratories and hospitals running GeneXpert instruments.
  • GeneXpert Xpertise Software Enterprise software platform for GeneXpert systems providing connectivity, data management, and workflow optimization across the installed base. Used by multi-site hospital networks and reference laboratories.
  • Cepheid C360 Connectivity solution enabling integration between GeneXpert systems and laboratory information systems. Used by hospital IT and laboratory informatics teams.
  • Xpert GI Panel FDA-cleared and CE-marked under IVDR multiplex PCR assay detecting 11 bacterial, viral, and parasitic gastrointestinal pathogens from a single stool specimen in approximately 74 minutes. Used by hospitals and clinical laboratories for infectious gastroenteritis testing.
  • Xpert MTB/RIF WHO-prequalified molecular test for tuberculosis detection that also identifies rifampicin resistance, providing results in approximately 90 minutes. Used by TB programs, hospitals, and public health laboratories globally.
  • Xpert Xpress MVP (Mpox) Molecular test for mpox (Monkeypox) virus detection. Used by public health laboratories and clinical labs responding to mpox outbreaks.
  • Xpert Xpress CoV-2/Flu/RSV plus Multiplex respiratory panel detecting SARS-CoV-2, influenza A/B, and RSV from a single sample with rapid turnaround. Used by hospitals, urgent care, and physician offices.
  • Xpert Xpress Flu/RSV Rapid multiplex test for influenza A, influenza B, and RSV detection. Used by physician offices, urgent care, and hospital labs.
  • Xpert Xpress Flu Rapid point-of-care test for influenza A and B. Used in physician offices, urgent care, and hospital point-of-care settings.
  • Xpert Xpress Strep A Rapid test for Group A Streptococcus detection from throat swab specimens. Used by physician offices, urgent care, and hospital point-of-care settings.
  • Xpert Xpress CoV-2 plus Rapid point-of-care PCR test for SARS-CoV-2 detection. Used by hospitals, urgent care, and physician offices.
  • Xpert SA Nasal Complete Test for Staphylococcus aureus and methicillin-resistant S. aureus (MRSA) screening from nasal specimens. Used by hospitals for pre-surgical and infection control screening.
  • Xpert MRSA/SA SSTI Test for MRSA and S. aureus detection from skin and soft tissue infections. Used by hospital infection control and emergency settings.
  • Xpert MRSA/SA Blood Culture Test for MRSA and S. aureus detection directly from positive blood cultures. Used by hospital microbiology laboratories for bloodstream infection workups.
  • Xpert MRSA NxG Next-generation MRSA screening test with enhanced performance characteristics. Used by hospitals for active surveillance and infection prevention.
  • Xpert C. difficile/Epi Test for Clostridioides difficile detection and ribotyping to identify epidemic strains. Used by hospitals and stewardship/infection control programs.
  • Xpert Norovirus Rapid molecular test for norovirus detection. Used by hospital laboratories during norovirus outbreaks.
  • Xpert vanA Test for vancomycin resistance gene (vanA) detection to identify Vancomycin-resistant Enterococcus (VRE). Used by hospital infection control and stewardship programs.
  • Xpert Carba-R Test for carbapenem resistance genes detection, supporting CPE screening programs. Used by hospital infection prevention and antimicrobial stewardship teams.
  • Xpert HCV FDA-authorized test using a 100 µL fingerstick blood sample for Hepatitis C virus detection at point of care. Used by public health programs, point-of-care settings, and outreach screening.
  • Xpert CT/NG Test for Chlamydia trachomatis and Neisseria gonorrhoeae detection. Used by sexual health clinics, hospitals, and reference laboratories.
  • Xpert GBS LB XC Test for Group B Streptococcus detection from Lim broth enriched samples for prenatal screening. Used by hospital labor and delivery and prenatal clinics.
  • Xpert Xpress GBS Rapid test for Group B Streptococcus detection. Used by hospital labor and delivery and prenatal point-of-care settings.
  • Xpert TV Test for Trichomonas vaginalis detection. Used by sexual health clinics, women's health providers, and clinical laboratories.
  • Xpert BCR-ABL Ultra Quantitative test for BCR-ABL fusion transcript monitoring in chronic myeloid leukemia (CML) patients. Used by hospital hematology/oncology labs and reference laboratories.
  • Xpert FII & FV Test for Factor II and Factor V Leiden mutations associated with thrombophilia. Used by clinical laboratories supporting hematology and prenatal genetics workflows.
  • Xpert Hemorrhagic Fever Panel Rapid molecular test detecting Ebola virus (including Bundibugyo strain), Crimean Congo hemorrhagic fever, Marburg, and Lassa viruses with results in approximately one hour. Used by public health agencies, ministries of health, and outbreak response teams.
  • Xpert MTB/XDR WHO-prequalified test detecting resistance to multiple TB drugs including isoniazid, ethionamide, fluoroquinolones, and second-line injectables, with results in about 90 minutes. Used by national TB programs and reference laboratories in high-burden settings.

Quantifiable outcome

  • Xpert GI Panel provides results in approximately 74 minutes compared to 48-72 hours for traditional culture methods
  • +3 more outcomes

Companies that use Cepheid

Customer profile

Named customers5 records

Segments4 records

Ideal customer profiles4 records

Cepheid technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature7 records

Cepheid partnerships and signals

Strategic signal

Partnerships

Seven partnerships are on record, tiered major and core.

  • U.S. GovernmentmajorGTM or Marketing Partner · 12 June 2026Cepheid coordinated with the U.S. government to support diagnostic response to the Ebola Bundibugyo outbreak in DRC and Uganda, following WHO's declaration as a Public Health Emergency of International Concern.
  • World Health Organization (WHO)majorGTM or Marketing Partner · 12 June 2026Cepheid coordinated with WHO to accelerate deployment and expand testing capacity for Ebola Bundibugyo outbreak response following the WHO's declaration of the outbreak as a Public Health Emergency of International Concern.
  • Africa Centres for Disease Control and PreventionmajorGTM or Marketing Partner · 12 June 2026Cepheid coordinated with Africa CDC to accelerate deployment and expand testing capacity for Ebola Bundibugyo outbreak response across affected regions.
  • Fleming InitiativecoreStrategic or Co-development Partner · 11 June 2026The Fleming Initiative (a partnership between Imperial College London and Imperial College Healthcare NHS Trust) and Cepheid launched the TRACE-CPE study, a two-and-a-half-year research project evaluating rapid molecular screening for carbapenemase-producing Enterobacterales (CPE) drug-resistant bacteria in NHS hospitals. The study compares one-hour rapid diagnostics against standard 48-hour culture-based methods to assess clinical, infection control, and cost impacts.
  • U.S. CDCcoreStrategic or Co-development Partner · 18 February 2026Cepheid was selected by the U.S. CDC as one of four national collaborators under a federal IDIQ contract to accelerate development and deployment of rapid diagnostic technologies during public health emergencies. The collaboration grants Cepheid early access to outbreak samples, genomic sequences, and critical reference materials to accelerate next-generation diagnostic assay creation. The partnership builds on Cepheid's track record including the launch of the first point-of-care PCR test for SARS-CoV-2 in the United States.
  • Oxford Nanopore TechnologiescoreStrategic or Co-development Partner · 1 May 2025Cepheid and Oxford Nanopore Technologies have expanded their partnership to phase two, building on successful phase one collaboration that produced a beta workflow for bacterial and fungal pathogen profiling in sepsis and bloodstream infection research. The updated workflow enables pathogen identification, antimicrobial resistance profiling, and genomic antibiotic susceptibility testing predictions, with a co-commercialized RUO launch planned for Q3-2026. Both companies share a long-term ambition to deliver an end-to-end in vitro diagnostic solution for complex infectious diseases.
  • OncoMark Ltd.coreStrategic or Co-development Partner · 16 December 2021Cepheid acquired OncoMark Ltd., a UCD spin-out company that developed the OncoMasTR test for breast cancer. The test is aimed at reducing unnecessary chemotherapy and will be launched on Cepheid's GeneXpert platform in global markets.

Scale indicators3 records

Recent moves7 records

Expansion highlights6 records

Cepheid competitors and assessment

Company assessment

Broad incumbents

  • Roche Diagnostics: Operates the cobas Liat (POC), cobas 6800/8800 (high-throughput), and broader molecular diagnostics menu. Comparable as a broad incumbent with overlapping PCR multiplex and point-of-care molecular capabilities competing for the same hospital and reference-lab customers.
  • Abbott: m-PIMA and ID NOW platforms compete in point-of-care molecular diagnostics, with Abbott leveraging a far broader diagnostics portfolio and global sales reach to pressure Cepheid in both POC and central-lab settings.
  • Becton Dickinson (BD): BD MAX system and BD Veritor offer molecular and rapid diagnostics that overlap with GeneXpert menu categories. Competes broadly across HAI, women's health, and respiratory testing with a larger installed base of hospital customers.
  • DiaSorin: Acquired Luminex and now offers multiplex molecular and immunoassay platforms. Competes in syndromic respiratory testing and broader hospital diagnostics where Cepheid's GeneXpert menu is sold.

Direct peers

  • Hologic: Panther Fusion and Aptima molecular diagnostics franchises compete head-to-head with GeneXpert in women's health, STI, and respiratory testing. Closely aligned business model (instrument + cartridge consumables) and overlapping hospital customer base.
  • bioMérieux: BioFire FilmArray syndromic panels directly compete with Cepheid's multiplex respiratory and GI panels. Same POC-to-lab workflow, similar customer base in hospital microbiology, and comparable regulatory pathway (FDA-cleared cartridge-based multiplex PCR).
  • Qiagen: QIAstat-Dx is a direct multiplex cartridge-based PCR competitor to GeneXpert, particularly in respiratory and GI testing. Comparable cartridge consumables model, regulatory positioning, and target hospital/urgent-care customer base.

Emerging players

  • Accelerate Diagnostics: Specializes in rapid identification and antimicrobial susceptibility testing (e.g., Pheno system), partially overlapping with Cepheid's Xpert Carba-R and antibiotic stewardship offerings. Smaller and more focused, but addresses the same AMR clinical workflow.
  • T2 Biosystems: T2 Magnetic Resonance-based direct-from-blood molecular diagnostics for sepsis pathogens. Targets a similar rapid molecular sepsis use case as Cepheid's emerging bloodstream infection workflow with Oxford Nanopore.

Others

  • Oxford Nanopore Technologies: Sequencing platform partner rather than a direct competitor, but a strategic adjacency: a successful Phase 2 co-developed sepsis/BSI workflow could become a future substitute for cartridge-based multiplex PCR, making Nanopore a peer by category as much as by partnership.

Market position

Strengths4 records

Weaknesses4 records

Competitive moat6 records

Key risks5 records

Key highlights6 records

Customer concentration

Cepheid social profiles

Digital presence

Cepheid compliance and trust

Trust signal

Compliance2 records

Cepheid financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Cepheid leadership team

Management profile

Number of profiles

Profiles13 records

Cepheid subsidiaries and ownership

Company hierarchy

Subsidiaries1 record

Cepheid funding detail

Funding detail

Funding overview

Funding rounds7 records

Investors5 records

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

Cepheid M&A and investment

M&A and investment

M&A1 record

Investments

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

Frequently asked questions about Cepheid

What does Cepheid do?

Cepheid develops, manufactures, and sells the GeneXpert family of automated real-time PCR molecular diagnostic instruments (GeneXpert System, GeneXpert Infinity, GeneXpert Xpress) and a broad menu of single-use Xpert test cartridges for respiratory infections, hospital-acquired infections, tuberculosis and emerging infectious diseases, blood virology/women's health/sexual health, and oncology/human genetics. Results are typically delivered in about one hour from specimen to answer, supported by GeneXpert Dx Software, GeneXpert Xpertise Software, and Cepheid C360 connectivity solutions.

Is Cepheid a public or private company?

Cepheid is a private company. It is classified as corporate owned and is currently operating.

When was Cepheid founded?

Cepheid was founded in 1996. It employs 5,001 to 10,000 people.

Where is Cepheid based?

Cepheid is headquartered in Sunnyvale, United States, in the North America region.

How does Cepheid make money?

Two revenue lines are on record. Molecular Diagnostics Instruments are the primary driver. The others are diagnostic Test Reagents and Cartridges.

Who are Cepheid's main competitors?

Broad incumbents on record are Roche Diagnostics, Abbott, Becton Dickinson (BD) and DiaSorin. Direct peers are Hologic, bioMérieux and Qiagen. Emerging players are Accelerate Diagnostics and T2 Biosystems. Oxford Nanopore Technologies is listed as an others.

Does Cepheid have an API?

No public API is recorded for Cepheid.

What industry is Cepheid in?

Cepheid's product category is Molecular Diagnostics. Its primary akta.pro industry code is HLAHAAAD, Molecular Diagnostics (PCR/NAAT/NGS-based IVD), with a secondary code of HLAAALAA, Molecular Diagnostics (PCR/qPCR, NGS-based assays). Its NAICS code is 3391 and its SIC code is 2835.

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Live signals
Medical Device NetworkFDA clears Cepheid’s multiplex respiratory panel testThe FDA cleared Cepheid's Xpert Respiratory Panel, a multiplex PCR test that identifies 13 common bacterial and viral respiratory pathogens from one nasopharyngeal swab. The panel is intended for patients with suspected respiratory tract infections and will be shipped to US customers in coming weeks.YahooFDA clears Cepheid’s multiplex respiratory panel testThe FDA cleared Cepheid's Xpert Respiratory Panel, a multiplex PCR test that detects 13 bacterial and viral respiratory pathogens from one nasopharyngeal swab. The panel is intended for patients with suspected respiratory infections and will be shipped to US customers in coming weeks.PR NewswireCepheid Receives FDA Clearance for Xpert® Respiratory Panel to Aid in the Diagnosis of Respiratory Tract InfectionCepheid received FDA clearance for its Xpert Respiratory Panel, a multiplex PCR test that detects 13 common viral and bacterial respiratory pathogens from a single nasopharyngeal swab. The test is intended to aid diagnosis of respiratory tract infections and will begin shipping to U.S. customers in the coming weeks.PR NewswirePCR Technologies Market worth $21.43 billion by 2031 - Exclusive Report by MarketsandMarkets™The PCR technologies market is projected to grow from $15.55 billion in 2026 to $21.43 billion by 2031, a CAGR of 6.6%. North America held the largest share at 45% in 2025, and reagents and consumables accounted for 65% of the market. Digital PCR is expected to see the highest CAGR of 9.5%.YahooWHO greenlights Cepheid’s Ebola diagnostic amid ongoing Bundibugyo outbreakWHO granted an emergency use listing to Cepheid's haemorrhagic fever panel for detecting the Bundibugyo Ebola virus strain. The listing follows a DRC outbreak with 6,186 cases and 3,007 deaths as of August 31. The test is the fourth diagnostic to receive an EUL for Ebola viruses.Medical Device NetworkWHO greenlights Cepheid’s Ebola diagnostic amid ongoing Bundibugyo outbreakThe WHO granted an emergency use listing to Cepheid's GeneXpert Dx for detecting Bundibugyo Ebola virus, the fourth such diagnostic since the outbreak was declared a public emergency in May 2026. The outbreak in the DRC has reported 6,186 cases and 3,007 deaths as of 31 August. WHO is accelerating antiviral and vaccine trials, including a Phase I trial for Moderna's mRNA-1469 candidate.AInvestWho Grants Cepheid's Emergency Use Listing — and Why the Headline Overrates ItThe World Health Organization granted Cepheid's Bundibugyo virus test an Emergency Use Listing, distinct from the FDA's Emergency Use Authorization. The EUL enables global procurement during crises but lacks commercial value in developed markets, and Cepheid's razor-and-blades model relies on recurring cartridge sales, not emergency approvals. For Danaher investors, the listing confirms platform credibility but has minimal financial impact compared to installed instrument growth.AInvestDanaher: Cepheid's WHO Ebola Listing Is a Real Asset, Not a Reason to BuyCepheid's WHO Emergency Use Listing for its Ebola test is described as immaterial to Danaher's valuation. The listing enables procurement but does not add recurring revenue, while Danaher trades at a full-quality multiple. The author sees no reason to change the stock rating.AInvestCepheid's WHO Emergency-Use Listing: Real Capability, Not a Revenue EngineCepheid will donate its Xpert Hemorrhagic Fever panel tests to the WHO for the Ebola Bundibugyo outbreak, but the listing is a licensing lane, not a revenue source. Danaher's Diagnostics segment earned $2.5 billion in Q2, with respiratory testing revenue down 15% year-over-year. The durable growth comes from non-respiratory tests, not the emergency listing.AijournWHO Grants Emergency Use Listing for Cepheid’s Xpert® Hemorrhagic Fever Panel Test to Support Ebola Outbreak Response in the DRCCepheid received WHO Emergency Use Listing for its Xpert Hemorrhagic Fever Panel test to support the Ebola Bundibugyo outbreak in the DRC. The test detects Ebola, CCHF, Marburg, and Lassa viruses, with results in about one hour, and runs on Cepheid's GeneXpert Dx systems. The listing enables expanded diagnostic access for public health partners.