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Cerus

Full company profile

uuid0003mtl

Namestring
Cerus
Legal namestring
Cerus Corporation
Websiteurl
cerus.com
Company typeenum
Public
Founded yearint
1991
Descriptiontext

Cerus Corporation (NASDAQ: CERS) is a publicly traded biomedical products company founded in 1991 and headquartered in Concord, California, with European operations based in Amersfoort, Netherlands. The company develops and commercializes the INTERCEPT Blood System, a pathogen reduction platform that uses proprietary amotosalen (a psoralen-based compound) plus UVA illumination to inactivate viruses, bacteria, parasites, and residual leukocytes in platelets and plasma by crosslinking pathogen nucleic acids. INTERCEPT is the only pathogen reduction system with both CE mark and FDA approval for platelets and plasma, and the company has additionally secured FDA approval for the INTERCEPT Fibrinogen Complex (IFC) produced via INTERCEPT Cryoprecipitation, used in the treatment of massive hemorrhage. The platform is anchored on the next-generation INT200 LED illumination device (CE-marked March 2025) and is being extended to red blood cells via the RedeS/RETIS Phase 3 program and to lyophilized IFC (LyoIFC) for trauma care.

Cerus generates revenue primarily through recurring sales of single-use disposable pathogen reduction kits sold to blood centers, hospitals, and national blood services, paired with capital equipment (illuminators). FY2025 total revenue was $233.8 million (up 16% YoY) and product revenue was $206.1 million (up 14% YoY), with FY2026 product revenue guidance of $227-231 million and Q1 2026 product revenue up 24% YoY. The company has secured multi-year supply agreements and group purchasing contracts that anchor distribution — most notably with American Red Cross, Blood Centers of America (~50% of U.S. blood supply), and Établissement Français du Sang (~330,000 platelet units/year across France) — and operates a direct enterprise sales motion supported by two regional hubs. Non-dilutive capital has been a meaningful financing layer: a $248 million BARDA contract (2024) supports the INTERCEPT Red Blood Cell program and ~$25.2 million in cumulative DoD funding supports LyoIFC development.

Cerus has been operationally profitable on a non-GAAP adjusted EBITDA basis for eight consecutive quarters (Q2 2024 through Q1 2026), with FY2025 non-GAAP adjusted EBITDA of $9.5 million and GAAP net loss narrowing to $15.6 million. The company is in the midst of a planned leadership transition, with COO Vivek K. Jayaraman announced to succeed William "Obi" Greenman as President and CEO effective July 1, 2026, and Greenman moving to Executive Chairman. As of June 2026, Cerus had a market capitalization of approximately $542 million (stock price $2.59, +89% over the prior year) and had recently refinanced its capital structure with a new up-to-$110 million debt facility from MidCap Financial.

Short descriptiontext

Cerus Corporation (NASDAQ: CERS) is a publicly traded biomedical products company that develops and commercializes the INTERCEPT Blood System — the only pathogen reduction platform with both CE mark and FDA approval for platelets and plasma — selling single-use consumable kits and illumination devices to blood centers, hospitals, and national blood services in approximately 40 countries.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
501–1,000
akta.pro rankint
HeadquartersConcord, United States
HQ citystring
Concord
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
pathogen reduction systems, blood component safety, transfusion medicine devices, blood center consumables, biomedical blood products
Industry2 codes
1Blood Bank, Transfusion Medicine & Immunohematology
CodeHLAHAAAHPrimaryYes
2Plasma-Derived & Blood Products Distributors
CodeHLAIAJAJPrimaryNo
NAICS code2 codes
  • Blood and Organ Banks621991
  • Medical Laboratories621511
SIC code2 codes
  • In Vitro & In Vivo Diagnostic Substances2835
  • Surgical & Medical Instruments & Apparatus3841
Product category
Blood Safety / Pathogen Reduction Systems
Social media profiles1 record
GTM motion3 records

Each record includes

Type, Description, Source

Revenue model4 records
1INTERCEPT Blood System consumable kits
TypeHardware Sales
Description

Recurring consumable revenue from sale of single-use disposable pathogen reduction kits (processing sets, amotosalen, storage containers) used to treat platelet and plasma components at blood centers. Described as the core financial driver with growing demand; FY2025 product revenue of $206.1M was 14% growth, with Q1 2026 product revenue up 24% YoY to $53.7M.

cerus.com
2Illumination / processing devices (capital equipment)
TypeHardware Sales
Description

One-time and replacement sales of INTERCEPT illuminators (legacy devices and the next-generation INT200 LED illuminator) installed at blood centers and hospitals as the capital equipment base that consumes the recurring kits.

ad-hoc-news.de
3INTERCEPT Fibrinogen Complex (IFC) kits
TypeHardware Sales
Description

Sale of IFC kits to US blood centers producing Pathogen Reduced Cryoprecipitated Fibrinogen Complex; FY2025 IFC revenue ~$16.7M (up ~80% YoY) and Q1 2026 IFC volume growth of ~120% YoY. FY2026 IFC guidance $22–24M (later revised upward).

finance.yahoo.com
4Government / BARDA and DoD contract revenue
TypeProfessional Services
Description

Non-dilutive funding from US Department of Defense (~$25.2M cumulative for LyoIFC) and BARDA ($248M RBC contract in 2024) supporting R&D and clinical development of pathogen reduction programs including LyoIFC and INTERCEPT RBC.

synapse.patsnap.com
Marketing channels7 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels5 records

Each record includes

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

Cost components5 values
Supply Chain, Technology or R&D, Personnel, Operations, Marketing or Sales
Pricing details2 tiers
1Quote-based, not publicly disclosed
ModelOther
Notes

Pricing is negotiated bilaterally via multi-year supply contracts with blood centers and national blood services; no public price list.

es.uchealth.org
2Unit pricing on consumable kits + capital device sales
ModelUnit PricingBilling cadenceMulti-year contract
Notes

Recurring revenue from single-use disposable kits paired with sale/rental of illumination devices (legacy illuminator and INT200). Per third-party reporting, INTERCEPT platelets priced at approximately $685 per unit vs $550 standard (a ~$135 uplift).

es.uchealth.org
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 3 records shown
1INTERCEPT Blood System
Description

Cerus' flagship pathogen reduction system for platelets and plasma; the only pathogen reduction system with both CE mark and FDA approval for these two blood components.

cerus.com
+2 more records
Core offering1 text field

Cerus Corporation develops, manufactures, and commercializes the INTERCEPT Blood System, a proprietary pathogen reduction platform that uses amotosalen (a psoralen compound) plus UVA illumination to inactivate viruses, bacteria, parasites, and residual leukocytes in donated platelets and plasma. The company sells single-use disposable pathogen reduction kits together with capital illumination devices to blood centers, hospitals, and national blood services, and also produces INTERCEPT Fibrinogen Complex (IFC) for massive hemorrhage treatment.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 10 values shown
  • FY2025 total revenue $233.8M, up 16% YoY; product revenue $206.1M, up 14% YoY.
+9 more records
Product overview1 text field

Cerus offers a single integrated pathogen reduction platform — the INTERCEPT Blood System — built around amotosalen-based photochemical treatment with UVA illumination. The platform spans multiple blood component applications: the FDA- and CE-marked INTERCEPT Blood System for Platelets, the FDA- and CE-marked INTERCEPT Blood System for Plasma, and the U.S.-approved INTERCEPT Fibrinogen Complex (IFC) produced via INTERCEPT Cryoprecipitation. The next-generation INT200 LED-based illumination device is the hardware backbone for processing across components. The company is also developing the INTERCEPT Red Blood Cell System (under CE Mark review in Europe and Phase 3 RedeS study in the U.S.) and a lyophilized IFC (LyoIFC) for trauma hemorrhage care, expanding the platform beyond platelets and plasma into a comprehensive blood-component safety portfolio.

Product and service4 records
1INTERCEPT Blood System for Platelets
CategoryPathogen Reduction System
Description

A pathogen reduction system for platelet components that uses amotosalen and UVA light to inactivate viruses, bacteria, parasites, and residual white blood cells in donated platelets. The only pathogen reduction system with both CE mark and FDA approval for platelets. Sold to blood centers, hospitals, and national blood services as single-use disposable kits processed on INTERCEPT illuminators.

2INTERCEPT Blood System for Plasma
CategoryPathogen Reduction System
Description

A pathogen reduction system for plasma components that uses amotosalen and UVA light to inactivate a broad spectrum of pathogens. The only pathogen reduction system with both CE mark and FDA approval for plasma. Sold to blood centers, hospitals, and national blood services.

3INTERCEPT Fibrinogen Complex (IFC)
CategoryTherapeutic Blood Product
Description

FDA-approved Pathogen Reduced Cryoprecipitated Fibrinogen Complex therapeutic product for the treatment and control of bleeding, including massive hemorrhage, associated with fibrinogen deficiency. Produced by U.S. blood centers using the INTERCEPT Blood System for Cryoprecipitation.

4INT200 Illumination Device
CategoryCapital Medical Device
Description

Next-generation LED-based illumination device for the INTERCEPT Blood System that replaces older illuminators. Serves as the foundational hardware platform for processing INTERCEPT-treated platelet and plasma kits. U.S. FDA PMA submission targeted for mid-2026.

Scale indicator17 records

Each record includes

Type, Value, Description, Source

Partnership8 partners
Strategic tierFlagshipTypeChannel Partner/ Reseller/ DistributorAnnounced on2026-04-27
Description

New four-year supply agreement (April 2026) covering INTERCEPT Blood System for platelets and plasma plus the next-generation INT200 illumination device. EFS distributes ~330,000 platelet units/year across 13 regional centers in continental France and overseas territories (La Réunion, Guadeloupe, Martinique). INTERCEPT has been used in France since 2006 with nationwide rollout in 2017.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-01-22
Description

Collaboration on the INITIATE study (started January 2026) — the first prospective multicenter non-interventional safety study evaluating INTERCEPT-treated pathogen-inactivated platelet concentrates in routine clinical practice in Germany. DRK is the sponsor; the study aims to confirm safety profile and feasibility of system-wide adoption in the German healthcare system.

Strategic tierFlagshipTypeChannel Partner/ Reseller/ DistributorAnnounced on2025-12-10
Description

Group purchasing agreement (December 2025) expanding access to INTERCEPT pathogen reduction technology across 60+ US blood centers representing approximately 50% of the U.S. blood supply. Includes collaborative training and resource sharing.

4European Notified Body (EU MDR)
Strategic tierCoreTypeOthersAnnounced on2025-03-09
Description

Regulatory partnership — receipt of CE Mark for the next-generation INT200 illumination device under EU Medical Device Regulation (March 2025), completing authorization of the INTERCEPT Blood System for both platelets and plasma within the EU MDR framework and enabling commercial distribution across the EU and CE-mark-recognizing regions.

marketscreener.com
Strategic tierMinorTypeOEM/ Whitelabel/ Licensing PartnerAnnounced on2024-12-08
Description

Extended supply agreement (December 2024) covering proprietary components used in Cerus' INTERCEPT disposable kits. Supports continuity of consumable kit supply for INTERCEPT-treated platelets and plasma.

Strategic tierFlagshipTypeStrategic or Co-development PartnerAnnounced on2024-11-01
Description

$248 million contract awarded (October 2024) to support development of Cerus' INTERCEPT Red Blood Cell program in the United States. Funding supports advancement of the RBC pathogen reduction system through clinical and regulatory milestones, complementing the RedeS/RETIS Phase 3 program.

Strategic tierFlagshipTypeChannel Partner/ Reseller/ Distributor
Description

Largest provider of platelets in the U.S.; publicly committed to a complete pathogen-reduced platelet inventory using INTERCEPT ahead of the FDA bacterial contamination guidance deadline. American Red Cross leadership publicly endorsed pathogen reduction as the standard of care.

8Susan Stramer, Ph.D. (American Red Cross VP Scientific Affairs)
Strategic tierMinorTypeGTM or Marketing Partner
Description

Featured expert on Cerus' Sepsis Webinar Series and in co-branded podcast 'Preparing Our Blood Supply for the Next Pandemic', jointly advancing the case for proactive pathogen reduction in the U.S. blood supply.

cerus.com
Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeEmerging player
Description

Immucor specializes in transfusion and transplantation diagnostics (blood typing, antigen detection) and sells into many of the same hospital blood banks as Cerus, providing adjacent — rather than directly competing — tools used alongside pathogen-reduced components.

TypeOthers
Description

Revvity (formerly PerkinElmer Life Sciences) supplies donor screening reagents, blood bank quality controls, and molecular diagnostics used in blood safety workflows. It is an ecosystem participant and adjacent technology supplier rather than a direct competitor to Cerus' pathogen reduction consumables.

TypeDirect peer
Description

Terumo's blood component technologies division develops the Mirasol Pathogen Reduction Technology system for platelets and plasma, the most directly comparable competing pathogen reduction platform to Cerus' INTERCEPT. Both target nucleic-acid-based pathogen inactivation in blood centers under regulated healthcare sales motions.

TypeBroad incumbent
Description

Grifols is a global blood products and transfusion medicine company (plasma fractionation, blood typing reagents, donor screening via Procleix) that operates broadly across the same blood safety value chain as Cerus, including nucleic-acid-testing blood screening assays that historically competed with the pathogen reduction concept.

TypeBroad incumbent
Description

Baxter is a broad incumbent in hospital products and transfusion medicine (IV solutions, blood storage/banking devices) and was previously a major employer of Cerus executives; it overlaps with Cerus as a hospital blood-bank supplier though it does not directly compete in pathogen reduction chemistry.

TypeBroad incumbent
Description

Haemonetics is a broad incumbent in transfusion medicine and blood center software/hardware (apheresis devices, platelet collection, donor management software), serving many of the same blood center customers as Cerus. While Haemonetics does not directly compete in pathogen reduction chemistry, it is a multi-product platform customer alternative for blood centers.

TypeRegional player
Description

Octapharma is one of the world's largest plasma fractionators and produces plasma-derived therapeutics including fibrinogen concentrates (relevant to IFC's hemorrhage indication). It is a regional/global participant in downstream blood product markets where INTERCEPT Fibrinogen Complex competes for share in massive hemorrhage treatment.

TypeDirect peer
Description

MacoPharma markets the THERAFLEX UV-Platelet and THERAFLEX MB-Plasma pathogen reduction systems, competing with INTERCEPT at blood centers in Europe and other regulated markets. Both companies sell consumable kits paired with illumination/processing devices into national blood services via multi-year supply contracts.

TypeBroad incumbent
Description

Fresenius Kabi is a large medical device and transfusion medicine supplier (apheresis platforms, IV solutions, blood bank devices) that overlaps with Cerus in selling into hospital blood banks and blood centers; Dean Gregory, formerly President of Global Commercial Operations at Fresenius Kabi, recently joined Cerus' board.

TypeBroad incumbent
Description

Hologic provides the Panther system and blood screening assays (e.g., via Grifols/Procleix partnerships and its own molecular diagnostics) that historically competed with Cerus on the alternative donor-screening paradigm for blood safety — a complementary/competing approach to INTERCEPT's single-procedure inactivation.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat7 records

Each record includes

Type, Details

Key risks7 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers7 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 profile3 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
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

Compliance3 records

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds6 records

Each record includes

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

Investors2 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 →

Cerus

Blood Safety / Pathogen Reduction Systemscerus.com

Cerus Corporation (NASDAQ: CERS) is a publicly traded biomedical products company that develops and commercializes the INTERCEPT Blood System — the only pathogen reduction platform with both CE mark and FDA approval for platelets and plasma — selling single-use consumable kits and illumination devices to blood centers, hospitals, and national blood services in approximately 40 countries.

What Cerus does

Cerus Corporation (NASDAQ: CERS) is a publicly traded biomedical products company founded in 1991 and headquartered in Concord, California, with European operations based in Amersfoort, Netherlands. The company develops and commercializes the INTERCEPT Blood System, a pathogen reduction platform that uses proprietary amotosalen (a psoralen-based compound) plus UVA illumination to inactivate viruses, bacteria, parasites, and residual leukocytes in platelets and plasma by crosslinking pathogen nucleic acids. INTERCEPT is the only pathogen reduction system with both CE mark and FDA approval for platelets and plasma, and the company has additionally secured FDA approval for the INTERCEPT Fibrinogen Complex (IFC) produced via INTERCEPT Cryoprecipitation, used in the treatment of massive hemorrhage. The platform is anchored on the next-generation INT200 LED illumination device (CE-marked March 2025) and is being extended to red blood cells via the RedeS/RETIS Phase 3 program and to lyophilized IFC (LyoIFC) for trauma care.

Cerus generates revenue primarily through recurring sales of single-use disposable pathogen reduction kits sold to blood centers, hospitals, and national blood services, paired with capital equipment (illuminators). FY2025 total revenue was $233.8 million (up 16% YoY) and product revenue was $206.1 million (up 14% YoY), with FY2026 product revenue guidance of $227-231 million and Q1 2026 product revenue up 24% YoY. The company has secured multi-year supply agreements and group purchasing contracts that anchor distribution — most notably with American Red Cross, Blood Centers of America (~50% of U.S. blood supply), and Établissement Français du Sang (~330,000 platelet units/year across France) — and operates a direct enterprise sales motion supported by two regional hubs. Non-dilutive capital has been a meaningful financing layer: a $248 million BARDA contract (2024) supports the INTERCEPT Red Blood Cell program and ~$25.2 million in cumulative DoD funding supports LyoIFC development.

Cerus has been operationally profitable on a non-GAAP adjusted EBITDA basis for eight consecutive quarters (Q2 2024 through Q1 2026), with FY2025 non-GAAP adjusted EBITDA of $9.5 million and GAAP net loss narrowing to $15.6 million. The company is in the midst of a planned leadership transition, with COO Vivek K. Jayaraman announced to succeed William "Obi" Greenman as President and CEO effective July 1, 2026, and Greenman moving to Executive Chairman. As of June 2026, Cerus had a market capitalization of approximately $542 million (stock price $2.59, +89% over the prior year) and had recently refinanced its capital structure with a new up-to-$110 million debt facility from MidCap Financial.

Cerus firmographics

Firmographics
Name
Cerus
Legal name
Cerus Corporation
Website
https://cerus.com
Company type
Public
Founded year
1991
Operating status
Operating
Headcount range
501–1,000 employees
Short description
Cerus Corporation (NASDAQ: CERS) is a publicly traded biomedical products company that develops and commercializes the INTERCEPT Blood System — the only pathogen reduction platform with both CE mark and FDA approval for platelets and plasma — selling single-use consumable kits and illumination devices to blood centers, hospitals, and national blood services in approximately 40 countries.
Ownership category
akta.pro rank

Cerus industry classification

Industry
Product category
Blood Safety / Pathogen Reduction Systems
NAICS
Blood and Organ Banks (621991), Medical Laboratories (621511)
SIC
In Vitro & In Vivo Diagnostic Substances (2835), Surgical & Medical Instruments & Apparatus (3841)
akta.pro primary industry
Blood Bank, Transfusion Medicine & Immunohematology (HLAHAAAH)
akta.pro secondary industry
Plasma-Derived & Blood Products Distributors (HLAIAJAJ)

Keywords

  • Pathogen reduction systems
  • Blood component safety
  • Transfusion medicine devices
  • Blood center consumables
  • Biomedical blood products

Where Cerus is headquartered

Location

Headquarters

HQ city
Concord
HQ country
United States
HQ region
North America

Offices2 records

Markets served

Cerus 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

Revenue model

  1. INTERCEPT Blood System consumable kits: Recurring consumable revenue from sale of single-use disposable pathogen reduction kits (processing sets, amotosalen, storage containers) used to treat platelet and plasma components at blood centers. Described as the core financial driver with growing demand; FY2025 product revenue of $206.1M was 14% growth, with Q1 2026 product revenue up 24% YoY to $53.7M.
  2. Illumination / processing devices (capital equipment): One-time and replacement sales of INTERCEPT illuminators (legacy devices and the next-generation INT200 LED illuminator) installed at blood centers and hospitals as the capital equipment base that consumes the recurring kits.
  3. INTERCEPT Fibrinogen Complex (IFC) kits: Sale of IFC kits to US blood centers producing Pathogen Reduced Cryoprecipitated Fibrinogen Complex; FY2025 IFC revenue ~$16.7M (up ~80% YoY) and Q1 2026 IFC volume growth of ~120% YoY. FY2026 IFC guidance $22–24M (later revised upward).
  4. Government / BARDA and DoD contract revenue: Non-dilutive funding from US Department of Defense (~$25.2M cumulative for LyoIFC) and BARDA ($248M RBC contract in 2024) supporting R&D and clinical development of pathogen reduction programs including LyoIFC and INTERCEPT RBC.

Pricing tiers

ModelBillingPrice
Other—Quote-based, not publicly disclosed
Unit PricingMulti-year contractUnit pricing on consumable kits + capital device sales

Go-to-market motion3 records

Distribution channels5 records

Marketing channels7 records

Cerus product offering

Product offering

Core offering

Cerus Corporation develops, manufactures, and commercializes the INTERCEPT Blood System, a proprietary pathogen reduction platform that uses amotosalen (a psoralen compound) plus UVA illumination to inactivate viruses, bacteria, parasites, and residual leukocytes in donated platelets and plasma. The company sells single-use disposable pathogen reduction kits together with capital illumination devices to blood centers, hospitals, and national blood services, and also produces INTERCEPT Fibrinogen Complex (IFC) for massive hemorrhage treatment.

Product overview

Cerus offers a single integrated pathogen reduction platform — the INTERCEPT Blood System — built around amotosalen-based photochemical treatment with UVA illumination. The platform spans multiple blood component applications: the FDA- and CE-marked INTERCEPT Blood System for Platelets, the FDA- and CE-marked INTERCEPT Blood System for Plasma, and the U.S.-approved INTERCEPT Fibrinogen Complex (IFC) produced via INTERCEPT Cryoprecipitation. The next-generation INT200 LED-based illumination device is the hardware backbone for processing across components. The company is also developing the INTERCEPT Red Blood Cell System (under CE Mark review in Europe and Phase 3 RedeS study in the U.S.) and a lyophilized IFC (LyoIFC) for trauma hemorrhage care, expanding the platform beyond platelets and plasma into a comprehensive blood-component safety portfolio.

Differentiator

Problem solved

Functional benefit

Brands

  • INTERCEPT Blood System: Cerus' flagship pathogen reduction system for platelets and plasma; the only pathogen reduction system with both CE mark and FDA approval for these two blood components.
  • INTERCEPT Fibrinogen Complex (IFC)
  • INT200

Products and services

  • INTERCEPT Blood System for Platelets A pathogen reduction system for platelet components that uses amotosalen and UVA light to inactivate viruses, bacteria, parasites, and residual white blood cells in donated platelets. The only pathogen reduction system with both CE mark and FDA approval for platelets. Sold to blood centers, hospitals, and national blood services as single-use disposable kits processed on INTERCEPT illuminators.
  • INTERCEPT Blood System for Plasma A pathogen reduction system for plasma components that uses amotosalen and UVA light to inactivate a broad spectrum of pathogens. The only pathogen reduction system with both CE mark and FDA approval for plasma. Sold to blood centers, hospitals, and national blood services.
  • INTERCEPT Fibrinogen Complex (IFC) FDA-approved Pathogen Reduced Cryoprecipitated Fibrinogen Complex therapeutic product for the treatment and control of bleeding, including massive hemorrhage, associated with fibrinogen deficiency. Produced by U.S. blood centers using the INTERCEPT Blood System for Cryoprecipitation.
  • INT200 Illumination Device Next-generation LED-based illumination device for the INTERCEPT Blood System that replaces older illuminators. Serves as the foundational hardware platform for processing INTERCEPT-treated platelet and plasma kits. U.S. FDA PMA submission targeted for mid-2026.

Quantifiable outcome

  • FY2025 total revenue $233.8M, up 16% YoY; product revenue $206.1M, up 14% YoY.
  • +9 more outcomes

Companies that use Cerus

Customer profile

Named customers7 records

Segments4 records

Ideal customer profiles3 records

Cerus technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature6 records

Cerus partnerships and signals

Strategic signal

Partnerships

Eight partnerships are on record, tiered flagship, core and minor.

  • Établissement Français du Sang (EFS)flagshipChannel Partner/ Reseller/ Distributor · 27 April 2026New four-year supply agreement (April 2026) covering INTERCEPT Blood System for platelets and plasma plus the next-generation INT200 illumination device. EFS distributes ~330,000 platelet units/year across 13 regional centers in continental France and overseas territories (La Réunion, Guadeloupe, Martinique). INTERCEPT has been used in France since 2006 with nationwide rollout in 2017.
  • German Red Cross Blood Donation Service Baden-Württemberg – Hessen (with subsidiary DRK Blood Donation Service North-East)coreStrategic or Co-development Partner · 22 January 2026Collaboration on the INITIATE study (started January 2026) — the first prospective multicenter non-interventional safety study evaluating INTERCEPT-treated pathogen-inactivated platelet concentrates in routine clinical practice in Germany. DRK is the sponsor; the study aims to confirm safety profile and feasibility of system-wide adoption in the German healthcare system.
  • Blood Centers of America (BCA)flagshipChannel Partner/ Reseller/ Distributor · 10 December 2025Group purchasing agreement (December 2025) expanding access to INTERCEPT pathogen reduction technology across 60+ US blood centers representing approximately 50% of the U.S. blood supply. Includes collaborative training and resource sharing.
  • European Notified Body (EU MDR)coreOthers · 9 March 2025Regulatory partnership — receipt of CE Mark for the next-generation INT200 illumination device under EU Medical Device Regulation (March 2025), completing authorization of the INTERCEPT Blood System for both platelets and plasma within the EU MDR framework and enabling commercial distribution across the EU and CE-mark-recognizing regions.
  • Porex (Porex Technologies)minorOEM/ Whitelabel/ Licensing Partner · 8 December 2024Extended supply agreement (December 2024) covering proprietary components used in Cerus' INTERCEPT disposable kits. Supports continuity of consumable kit supply for INTERCEPT-treated platelets and plasma.
  • BARDA (Biomedical Advanced Research and Development Authority, U.S. HHS)flagshipStrategic or Co-development Partner · 1 November 2024$248 million contract awarded (October 2024) to support development of Cerus' INTERCEPT Red Blood Cell program in the United States. Funding supports advancement of the RBC pathogen reduction system through clinical and regulatory milestones, complementing the RedeS/RETIS Phase 3 program.
  • American Red CrossflagshipChannel Partner/ Reseller/ DistributorLargest provider of platelets in the U.S.; publicly committed to a complete pathogen-reduced platelet inventory using INTERCEPT ahead of the FDA bacterial contamination guidance deadline. American Red Cross leadership publicly endorsed pathogen reduction as the standard of care.
  • Susan Stramer, Ph.D. (American Red Cross VP Scientific Affairs)minorGTM or Marketing PartnerFeatured expert on Cerus' Sepsis Webinar Series and in co-branded podcast 'Preparing Our Blood Supply for the Next Pandemic', jointly advancing the case for proactive pathogen reduction in the U.S. blood supply.

Scale indicators17 records

Recent moves6 records

Expansion highlights6 records

Cerus competitors and assessment

Company assessment

Emerging players

  • Immucor: Immucor specializes in transfusion and transplantation diagnostics (blood typing, antigen detection) and sells into many of the same hospital blood banks as Cerus, providing adjacent — rather than directly competing — tools used alongside pathogen-reduced components.

Others

  • Revvity: Revvity (formerly PerkinElmer Life Sciences) supplies donor screening reagents, blood bank quality controls, and molecular diagnostics used in blood safety workflows. It is an ecosystem participant and adjacent technology supplier rather than a direct competitor to Cerus' pathogen reduction consumables.

Direct peers

  • Terumo BCT: Terumo's blood component technologies division develops the Mirasol Pathogen Reduction Technology system for platelets and plasma, the most directly comparable competing pathogen reduction platform to Cerus' INTERCEPT. Both target nucleic-acid-based pathogen inactivation in blood centers under regulated healthcare sales motions.
  • MacoPharma: MacoPharma markets the THERAFLEX UV-Platelet and THERAFLEX MB-Plasma pathogen reduction systems, competing with INTERCEPT at blood centers in Europe and other regulated markets. Both companies sell consumable kits paired with illumination/processing devices into national blood services via multi-year supply contracts.

Broad incumbents

  • Grifols: Grifols is a global blood products and transfusion medicine company (plasma fractionation, blood typing reagents, donor screening via Procleix) that operates broadly across the same blood safety value chain as Cerus, including nucleic-acid-testing blood screening assays that historically competed with the pathogen reduction concept.
  • Baxter International: Baxter is a broad incumbent in hospital products and transfusion medicine (IV solutions, blood storage/banking devices) and was previously a major employer of Cerus executives; it overlaps with Cerus as a hospital blood-bank supplier though it does not directly compete in pathogen reduction chemistry.
  • Haemonetics Corporation: Haemonetics is a broad incumbent in transfusion medicine and blood center software/hardware (apheresis devices, platelet collection, donor management software), serving many of the same blood center customers as Cerus. While Haemonetics does not directly compete in pathogen reduction chemistry, it is a multi-product platform customer alternative for blood centers.
  • Fresenius Kabi: Fresenius Kabi is a large medical device and transfusion medicine supplier (apheresis platforms, IV solutions, blood bank devices) that overlaps with Cerus in selling into hospital blood banks and blood centers; Dean Gregory, formerly President of Global Commercial Operations at Fresenius Kabi, recently joined Cerus' board.
  • Hologic: Hologic provides the Panther system and blood screening assays (e.g., via Grifols/Procleix partnerships and its own molecular diagnostics) that historically competed with Cerus on the alternative donor-screening paradigm for blood safety — a complementary/competing approach to INTERCEPT's single-procedure inactivation.

Regional players

  • Octapharma: Octapharma is one of the world's largest plasma fractionators and produces plasma-derived therapeutics including fibrinogen concentrates (relevant to IFC's hemorrhage indication). It is a regional/global participant in downstream blood product markets where INTERCEPT Fibrinogen Complex competes for share in massive hemorrhage treatment.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat7 records

Key risks7 records

Key highlights7 records

Customer concentration

Cerus social profiles

Digital presence

Cerus compliance and trust

Trust signal

Compliance3 records

Cerus financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Cerus leadership team

Management profile

Number of profiles

Profiles13 records

Cerus subsidiaries and ownership

Company hierarchy

Subsidiaries1 record

Cerus funding detail

Funding detail

Funding overview

Funding rounds6 records

Investors2 records

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Cerus M&A and investment

M&A and investment

M&A

Investments

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Frequently asked questions about Cerus

What does Cerus do?

Cerus Corporation develops, manufactures, and commercializes the INTERCEPT Blood System, a proprietary pathogen reduction platform that uses amotosalen (a psoralen compound) plus UVA illumination to inactivate viruses, bacteria, parasites, and residual leukocytes in donated platelets and plasma. The company sells single-use disposable pathogen reduction kits together with capital illumination devices to blood centers, hospitals, and national blood services, and also produces INTERCEPT Fibrinogen Complex (IFC) for massive hemorrhage treatment.

Is Cerus a public or private company?

Cerus is a public company. It is classified as public and is currently operating.

When was Cerus founded?

Cerus was founded in 1991. It employs 501 to 1,000 people.

Where is Cerus based?

Cerus is headquartered in Concord, United States, in the North America region.

How does Cerus make money?

Four revenue lines are on record. INTERCEPT Blood System consumable kits are the primary driver. The others are illumination / processing devices (capital equipment), INTERCEPT Fibrinogen Complex (IFC) kits and government / BARDA and DoD contract revenue.

Who are Cerus's main competitors?

Immucor is listed as an emerging player. Revvity is listed as an others. Direct peers are Terumo BCT and MacoPharma. Broad incumbents are Grifols, Baxter International, Haemonetics Corporation, Fresenius Kabi and Hologic. Octapharma is listed as a regional player.

Does Cerus have an API?

No public API is recorded for Cerus.

What industry is Cerus in?

Cerus's product category is Blood Safety / Pathogen Reduction Systems. Its primary akta.pro industry code is HLAHAAAH, Blood Bank, Transfusion Medicine & Immunohematology, with a secondary code of HLAIAJAJ, Plasma-Derived & Blood Products Distributors. Its NAICS code is 621991 and its SIC code is 2835.

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American Banking and Market NewsContrasting TransMedics Group (NASDAQ:TMDX) and Cerus (NASDAQ:CERS)Cerus and TransMedics Group are compared on profitability, valuation, risk, and analyst ratings. TransMedics has higher revenue and earnings, but Cerus trades at a lower P/E and has a higher consensus target price. Analysts favor Cerus, citing stronger upside potential.American Banking and Market NewsHead to Head Survey: Cerus (NASDAQ:CERS) versus Bausch + Lomb (NYSE:BLCO)Cerus and Bausch + Lomb are compared on institutional ownership, risk, profitability, and analyst ratings. Cerus has 78.4% institutional ownership versus 11.1% for Bausch + Lomb, and a beta of 1.83 versus 0.56. Cerus beats Bausch + Lomb on 9 of 14 factors, with a consensus price target of $5.25 implying 130.26% upside.American Banking and Market NewsCerus Corporation $CERS Shares Newly Acquired by Bank of America Corp DEBank of America Corp DE acquired a new stake in Cerus Corporation in Q2, buying 868,457 shares valued at about $2.5 million. Cerus reported Q2 EPS of -$0.01, meeting estimates, with revenue of $63.30 million. Analysts have a consensus 'Hold' rating with a $5.25 price target.Defense WorldRxSight (NASDAQ:RXST) & Cerus (NASDAQ:CERS) Critical AnalysisCerus and RxSight are compared on profitability, valuation, and analyst ratings. Cerus beats RxSight on 11 of 14 factors, with higher revenue and a lower price-to-earnings ratio. Analysts favor Cerus, citing a stronger consensus rating and higher potential upside.Investing.comCerus Corp chief legal officer sells $89,529 in company stock. By Investing.comChrystal Jensen, Chief Legal Officer at Cerus Corp, sold 30,000 shares worth $89,529 pursuant to a pre-arranged 10b5-1 trading plan on August 17, 2026. This transaction follows Cerus Corp's second-quarter 2026 financial results, where the company surpassed Wall Street expectations for profit and revenue but saw its stock drop due to margin pressure concerns.AInvestCathie Just Bought $CERS, Slipped Solana Into ARK, and Cut TXG - Is the FOMO Train Still Running?ARK Invest rotated its portfolio by purchasing 66,263 shares of Cerus Corp and acquiring Solana exposure via the 3iQ Solana Staking ETF, while simultaneously reducing its holdings in 10x Genomics. This strategic shift reflects a move toward entities with fresher near-term catalysts, citing Cerus's positive adjusted EBITDA and revenue growth alongside Solana's status as a major blockchain network. The trades indicate a downranking of 10x Genomics rather than a complete exit from the position.Defense WorldAssenagon Asset Management S.A. Has $920,000 Stock Holdings in Cerus Corporation $CERSAssenagon Asset Management S.A. reduced its stake in Cerus Corporation by 74.8% during the second quarter, selling over 936,000 shares. Concurrently, several other institutional investors established new positions in the biotechnology firm, while insiders sold shares to cover tax withholding obligations related to equity vesting.Markets DailyCerus (NASDAQ:CERS) Downgraded to “Hold” Rating by Wall Street ZenWall Street Zen downgraded Cerus stock from a buy to a hold rating, adding to a mixed landscape of analyst opinions that includes upgrades from BTIG Research and Zacks Research. The report also highlighted recent insider share sales by directors Eric Bjerkholt and Chrystal Jensen, as well as increased institutional holdings from firms such as Cubist Systematic Strategies and AQR Capital Management.Markets DailyWasatch Advisors LP Sells 1,897,237 Shares of Cerus Corporation $CERSWasatch Advisors LP reduced its stake in Cerus Corporation by 35.9% during the second quarter, selling nearly 1.9 million shares while other institutional investors such as AQR Capital Management and Cubist Systematic Strategies increased their positions. Analysts recently revised ratings on the biotechnology company's stock, with BTIG Research upgrading it to a 'buy' rating and setting a $4.00 price target. Insider sales were reported for tax withholding obligations, while the company recently reported quarterly earnings that met revenue expectations despite a net loss.AInvestCerus Q2 Beat, but Margins Dented: Why CERS Fell 15% and What Matters NextCerus Corporation reported Q2 revenue of $63.3 million, beating the $62.9 million forecast and raising full-year 2026 product revenue guidance to $229–$231 million, with product revenue up 10% year-over-year. Despite the beat, shares fell 15.21% to $2.45 after hours as investors focused on product gross margin compression to 51.4% from 55.2% a year earlier, raising concerns about the company's ability to convert growth into profit. The company posted its ninth consecutive quarter of positive adjusted EBITDA at $3.0 million and reduced its term loan by $30 million, though operating cash flow remained negative at $2.7 million.