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Cordis

Full company profile

uuid00058sf

Namestring
Cordis
Legal namestring
Cordis US Corp
Company typeenum
Private
Founded yearint
1959
Descriptiontext

Cordis is a privately held, private-equity-backed interventional cardiovascular medical device company founded in the late 1950s and headquartered in Miami Lakes, Florida, with regional headquarters in Zurich (EMEA) and Singapore (APAC). The company designs, manufactures, and sells drug-eluting balloons (SELUTION SLR), vascular closure devices (MYNX CONTROL, MYNXGRIP, EXOSEAL), self-expanding peripheral and carotid stents (S.M.A.R.T. RADIANZ, PRECISE PRO RX), AAA stent grafts (INCRAFT), vena cava filters (OPTEASE), embolic protection devices (ANGIOGUARD RX), re-entry catheters (OUTBACK Elite), and a broad portfolio of guidewires, diagnostic and guiding catheters, and PTA balloons. Its core technology is the proprietary MicroReservoir sirolimus-release platform combined with Cell Adherent Technology (CAT) on the SELUTION SLR drug-eluting balloon, which delivers sustained limus release for up to 90 days and is positioned as a "metal-free" alternative to drug-eluting stents across coronary and peripheral indications.

The company monetizes primarily through direct sales of hardware devices to hospitals, interventional cardiologists, vascular surgeons, and electrophysiologists across more than 70 countries, with SELUTION SLR commercially available in 65+ countries and investigational in the United States. Pricing is negotiated regionally via direct sales teams, hospital contracts, and group purchasing organizations such as Premier, supplemented by medical education, fellowship grants, and investigator-initiated studies that drive adoption. Cordis is owned by Hellman & Friedman (lead) and KKR (co-investor), who acquired it from Cardinal Health in 2021 for approximately $1 billion, and the company has since deployed significant capital — most notably the up-to-$1.135 billion acquisition of MedAlliance (October 2023) — to position SELUTION SLR as a category-defining asset. Cordis-X, an independent innovation accelerator based in Menlo Park and operated in partnership with Ajax Health, sources next-generation technologies (including the Ladera Large Bore Closure System and the Endovascular Engineering thrombectomy investment) into the Cordis portfolio.

Short descriptiontext

Cordis is a privately held, PE-backed interventional cardiovascular medical device company that designs and sells drug-eluting balloons (SELUTION SLR), vascular closure devices, stents, and endovascular tools to hospitals and physicians across 70+ countries.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1,001–5,000
akta.pro rankint
HeadquartersHialeah, United States
HQ citystring
Hialeah
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices4 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
interventional cardiology devices, drug-eluting balloons, vascular closure devices, peripheral vascular stents, endovascular medical devices
Industry3 codes
1Coronary Stents & Drug-Eluting Technologies
CodeHLAHAFAAPrimaryYes
2Structural Heart Valves (TAVR/SAVR) & Valve Repair
CodeHLAHAFABPrimaryNo
3Vascular Access & Closure Devices (Sheaths, Guidewires, Closure Systems)
CodeHLAHAFAKPrimaryNo
NAICS code3 codes
  • Surgical and Medical Instrument Manufacturing339112
  • Electromedical and Electrotherapeutic Apparatus Manufacturing334510
  • Surgical Appliance and Supplies Manufacturing339113
SIC code3 codes
  • Surgical & Medical Instruments & Apparatus3841
  • Orthopedic, Prosthetic & Surgical Appliances & Supplies3842
  • Electromedical & Electrotherapeutic Apparatus3845
Product category
Interventional Cardiology & Endovascular Medical Devices
Social media profiles3 records
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model2 records
1Cardiovascular medical device sales
TypeHardware Sales
Description

Primary revenue stream from the sale of interventional cardiology and endovascular devices (drug-eluting balloons, vascular closure devices, stent systems, catheters, guidewires) to hospitals and healthcare providers globally across more than 60–70 countries.

cordis.com
2Medical education and grants programs
TypeProfessional Services
Description

Cordis supports independent medical education through fellowship grants, educational grants, and investigator-initiated studies, which support adoption of its commercial products but are not directly revenue-generating.

cordis.com
Marketing channels8 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
Operations, Personnel, Technology or R&D, Supply Chain, Marketing or Sales
Pricing details1 tier
1GPO / negotiated hospital pricing via Premier agreement
ModelOther
Notes

Pricing negotiated through Premier group purchasing organization for products including MYNX CONTROL Venous Vascular Closure Device; exact price points not publicly disclosed.

cardiovascularbusiness.com
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 4 records shown
1Cordis-X
Description

Independent innovation accelerator / growth engine for Cordis, focused on identifying, investing in, and developing next-generation medical device technologies for the Cordis portfolio.

cordis.com
+3 more records
Core offering1 text field

Cordis manufactures and sells a portfolio of interventional cardiovascular medical devices used by hospitals and physicians for the diagnosis and treatment of coronary and peripheral vascular disease. Its commercial offering spans drug-eluting balloons (SELUTION SLR PTCA and PTA platforms), vascular closure devices (MYNX CONTROL, MYNXGRIP, EXOSEAL), self-expanding and balloon-expandable stents (S.M.A.R.T. RADIANZ, INCRAFT AAA, PALMAZ BLUE, PRECISE), guidewires, diagnostic and guiding catheters, PTA dilatation catheters, embolic protection devices and transradial introducer sheaths. Cordis sells these devices to hospitals and healthcare systems in more than 70 countries through its own direct sales organizations in the Americas, EMEA and APAC.

Differentiator
Functional benefit
Problem solved
Product overview1 text field

Cordis offers a platform-plus-modules architecture spanning interventional cardiology and peripheral/endovascular interventions, organized across two main portfolios: (1) Interventional Cardiology, anchored by the SELUTION SLR PTCA Drug Eluting Balloon (DEB) using proprietary MicroReservoir sustained sirolimus release, supplemented by MYNX CONTROL / MYNXGRIP / EXOSEAL vascular closure devices, RAIN Sheath transradial introducers, and a full range of guidewires, diagnostic and guiding catheters, and PTCA balloons; and (2) Peripheral Interventions, anchored by the SELUTION SLR PTA Drug Eluting Balloon, the S.M.A.R.T. RADIANZ self-expanding peripheral stent, the BRITE TIP RADIANZ guiding sheath and SABERX RADIANZ PTA dilatation catheter (collectively marketed as the Radianz Radial Peripheral System), the INCRAFT AAA Stent Graft System, the OPTEASE Retrievable Vena Cava Filter, and a full lower-extremity, renal, carotid, and venous portfolio of catheter sheaths, guidewires, diagnostic catheters, and PTA balloons. Cross-cutting products include the ANGIOGUARD RX emboli protection guidewire and the OUTBACK Elite Re-Entry Catheter. Cordis-X serves as an independent innovation accelerator (in partnership with Ajax Health) sourcing new technologies such as the Ladera Large Bore Closure System. Cordis's historical leadership position is rooted in introducing the first guidewire, the first drug-eluting stent (CYPHER), and now the SELUTION SLR DEB platform following the October 2023 MedAlliance acquisition.

Product and service3 records
1SELUTION SLR PTCA Drug Eluting Balloon (DEB)
CategoryDrug-eluting balloon (coronary)
Description

Latest-generation sirolimus drug-eluting balloon for coronary interventions, using proprietary Cell Adherent Technology (CAT) and MicroReservoirs made from biodegradable polymer mixed with sirolimus to provide controlled and sustained drug release for up to 90 days, designed to deliver drug-eluting stent-equivalent performance without leaving a permanent metal implant.

2SELUTION SLR PTA Drug Eluting Balloon
CategoryDrug-eluting balloon (peripheral / lower extremity)
Description

Sirolimus drug-eluting balloon for peripheral (lower extremity / popliteal / SFA) interventions leveraging the MicroReservoir sustained-release technology. Used in the SELUTION SFA Japan Trial and SUCCESS PTA Study demonstrating up to 81.5% 3-year primary patency.

3RAIN Sheath Transradial Hydrophilic Thin-walled Introducer
Scale indicator12 records

Each record includes

Type, Value, Description, Source

Partnership8 partners
Strategic tierStrategic Public-Sector PartnerTypeOthersAnnounced on2026-03-17
Strategic tierProduct Innovation PartnershipTypeStrategic or Co-development PartnerAnnounced on2025-10-23
Description

Partnership between Cordis-X and Ladera Medical to develop the Ladera Large Bore Closure System, designed for quick, safe vascular closure after percutaneous catheterization. The FASTEN trial has enrolled its first 25 patients with the goal of obtaining CE Mark approval.

Strategic tierBackground Executive AffiliationTypeOthersAnnounced on2025-04-01
Description

Matthew Muscari, Cordis President of the Americas, previously led CSI's Peripheral Vascular Commercial organization before joining Cordis; not an active commercial partnership but reflects sector expertise and alumni network.

Strategic tierStrategic Cybersecurity VendorTypeTechnology or IntegrationAnnounced on2024-10-14
Description

Cordis partnered with Palo Alto Networks to deploy a cyber transformation initiative protecting patient data and blocking emerging threats across the enterprise. The collaboration was featured as a customer case study.

Strategic tierU.S. Gpo Distribution PartnershipTypeChannel Partner/ Reseller/ DistributorAnnounced on2024-07-18
Description

Cordis signed a pricing deal with Premier, a major U.S. healthcare group purchasing organization, simultaneously with FDA approval of the MYNX CONTROL Venous Vascular Closure Device. The agreement enables Premier's member hospitals to access Cordis products under negotiated pricing.

Strategic tierFlagship Acquisition / TransformationalTypeStrategic or Co-development PartnerAnnounced on2023-10-02
Description

Cordis completed the acquisition of Switzerland-based MedAlliance in October 2023 for up to $1.135 billion including milestone payments through 2029 (initial $35M investment, $200M closing payment, up to $125M regulatory milestones, up to $775M commercial milestones). MedAlliance's proprietary SELUTION SLR™ drug-eluting balloon technology is now central to Cordis's coronary and peripheral vascular portfolios, with over 40,000 SELUTION units used in patient treatment to date.

Strategic tierGrowth / Venous Thromboembolism Market ExpansionTypeStrategic or Co-development PartnerAnnounced on2022-04-05
Description

Cordis made a strategic investment in Endovascular Engineering (E2), a Menlo Park-based developer of next-generation thrombectomy devices for Deep Vein Thrombosis (DVT) and Pulmonary Embolism (PE). The investment expands Cordis's portfolio into the Venous Thromboembolism Market. E2 was founded in 2019 by Dr. Luis Savastano and is also backed by Santé Ventures and another strategic investor.

Strategic tierFlagship / Innovation Engine PartnerTypeStrategic or Co-development PartnerAnnounced on2021-01-01
Description

Ajax Health partnered with Cordis to lead and fund Cordis-X, Cordis's independent innovation accelerator. Ajax has over 20 years of experience developing medical devices, and Ajax-developed technologies have generated over $750 million in annual revenue for their acquirers and have been used to treat over one million patients. Ajax's CEO Duke Rohlen also serves as CEO of Cordis-X.

Recent move9 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight7 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

Global medical device leader with deep interventional cardiology and peripheral vascular portfolios including drug-eluting stents, balloons, and closure devices. Direct competitor to Cordis in DES, DEB, and vascular closure; serves the same hospitals and interventional cardiologists but at much larger scale.

TypeBroad incumbent
Description

Largest medical device company globally, with leading coronary stent (Resolute Onyx), drug-eluting balloon, and peripheral vascular franchises. Competes head-to-head with Cordis across PCI, peripheral, and AAA stent graft markets through its direct sales force and broad hospital contracts.

TypeBroad incumbent
Description

Major cardiovascular device player with Xience DES, peripheral intervention, and structural heart franchises. Competes with Cordis in coronary stents, imaging, and vascular closure through its large direct sales organization and global hospital footprint.

TypeBroad incumbent
Description

BD's Interventional segment (formerly Bard) includes peripheral stents, PTA balloons, drug-coated balloons, and vascular closure devices, directly overlapping Cordis's SFA, BTK, and closure device portfolios. BD's scale and GPO relationships make it one of Cordis's most direct incumbents.

TypeDirect peer
Description

Japanese medical device company with significant interventional cardiology and vascular closure offerings (e.g., TR Band, drug-eluting technologies through Terumo Medical). Competes with Cordis in transradial access sheaths, vascular closure, and coronary intervention products globally.

TypeEmerging player
Description

Specialist in intravascular lithotripsy (IVL) for calcium modification in coronary and peripheral interventions. Adjacent disruptor to Cordis's peripheral intervention portfolio; was acquired by Johnson & Johnson, raising competitive intensity in the peripheral space.

TypeEmerging player
Description

Focused on mechanical thrombectomy and vascular embolization, overlapping with Cordis's E2 investment and broader peripheral/venous portfolio. Competes in the VTE and peripheral arterial thrombectomy segments where Cordis is expanding.

TypeEmerging player
Description

Pure-play venous thromboembolism and venous intervention device company (acquired by Stryker). Overlaps with Cordis's E2 thrombectomy investment and the OPTEASE vena cava filter franchise in the venous intervention market.

TypeDirect peer
Description

Medical device company with vascular closure (e.g., MANTA large-bore closure), interventional cardiology, and peripheral vascular products. Directly competes with Cordis's MYNX CONTROL closure portfolio, particularly in the large-bore structural heart and endovascular space.

TypeEmerging player
Description

Mid-cap medical device company focused on peripheral vascular disease and venous intervention, with overlapping product lines in PTA balloons, thrombectomy, and venous access. Smaller scale than Cordis but competes in similar hospital accounts for peripheral intervention procedures.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 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 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 profile2 records

Each record includes

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

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature7 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles10 records

Each record includes

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

Subsidiaries3 records

Each record includes

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

Compliance4 records

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds

Each record includes

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

Investors

Each record includes

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

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

M&A4 records

Each record includes

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

Investment2 records

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 →

Cordis

Interventional Cardiology & Endovascular Medical Devicescordis.com

Cordis is a privately held, PE-backed interventional cardiovascular medical device company that designs and sells drug-eluting balloons (SELUTION SLR), vascular closure devices, stents, and endovascular tools to hospitals and physicians across 70+ countries.

What Cordis does

Cordis is a privately held, private-equity-backed interventional cardiovascular medical device company founded in the late 1950s and headquartered in Miami Lakes, Florida, with regional headquarters in Zurich (EMEA) and Singapore (APAC). The company designs, manufactures, and sells drug-eluting balloons (SELUTION SLR), vascular closure devices (MYNX CONTROL, MYNXGRIP, EXOSEAL), self-expanding peripheral and carotid stents (S.M.A.R.T. RADIANZ, PRECISE PRO RX), AAA stent grafts (INCRAFT), vena cava filters (OPTEASE), embolic protection devices (ANGIOGUARD RX), re-entry catheters (OUTBACK Elite), and a broad portfolio of guidewires, diagnostic and guiding catheters, and PTA balloons. Its core technology is the proprietary MicroReservoir sirolimus-release platform combined with Cell Adherent Technology (CAT) on the SELUTION SLR drug-eluting balloon, which delivers sustained limus release for up to 90 days and is positioned as a "metal-free" alternative to drug-eluting stents across coronary and peripheral indications.

The company monetizes primarily through direct sales of hardware devices to hospitals, interventional cardiologists, vascular surgeons, and electrophysiologists across more than 70 countries, with SELUTION SLR commercially available in 65+ countries and investigational in the United States. Pricing is negotiated regionally via direct sales teams, hospital contracts, and group purchasing organizations such as Premier, supplemented by medical education, fellowship grants, and investigator-initiated studies that drive adoption. Cordis is owned by Hellman & Friedman (lead) and KKR (co-investor), who acquired it from Cardinal Health in 2021 for approximately $1 billion, and the company has since deployed significant capital — most notably the up-to-$1.135 billion acquisition of MedAlliance (October 2023) — to position SELUTION SLR as a category-defining asset. Cordis-X, an independent innovation accelerator based in Menlo Park and operated in partnership with Ajax Health, sources next-generation technologies (including the Ladera Large Bore Closure System and the Endovascular Engineering thrombectomy investment) into the Cordis portfolio.

Cordis firmographics

Firmographics
Name
Cordis
Legal name
Cordis US Corp
Website
https://www.cordis.com/
Company type
Private
Founded year
1959
Operating status
Operating
Headcount range
1,001–5,000 employees
Short description
Cordis is a privately held, PE-backed interventional cardiovascular medical device company that designs and sells drug-eluting balloons (SELUTION SLR), vascular closure devices, stents, and endovascular tools to hospitals and physicians across 70+ countries.
Ownership category
akta.pro rank

Cordis industry classification

Industry
Product category
Interventional Cardiology & Endovascular Medical Devices
NAICS
Surgical and Medical Instrument Manufacturing (339112), Electromedical and Electrotherapeutic Apparatus Manufacturing (334510), Surgical Appliance and Supplies Manufacturing (339113)
SIC
Surgical & Medical Instruments & Apparatus (3841), Orthopedic, Prosthetic & Surgical Appliances & Supplies (3842), Electromedical & Electrotherapeutic Apparatus (3845)
akta.pro primary industry
Coronary Stents & Drug-Eluting Technologies (HLAHAFAA)
akta.pro secondary industries
Structural Heart Valves (TAVR/SAVR) & Valve Repair (HLAHAFAB), Vascular Access & Closure Devices (Sheaths, Guidewires, Closure Systems) (HLAHAFAK)

Keywords

  • Interventional cardiology devices
  • Drug-eluting balloons
  • Vascular closure devices
  • Peripheral vascular stents
  • Endovascular medical devices

Where Cordis is headquartered

Location

Headquarters

HQ city
Hialeah
HQ country
United States
HQ region
North America

Offices4 records

Markets served

Cordis business model

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

Revenue model

  1. Cardiovascular medical device sales: Primary revenue stream from the sale of interventional cardiology and endovascular devices (drug-eluting balloons, vascular closure devices, stent systems, catheters, guidewires) to hospitals and healthcare providers globally across more than 60–70 countries.
  2. Medical education and grants programs: Cordis supports independent medical education through fellowship grants, educational grants, and investigator-initiated studies, which support adoption of its commercial products but are not directly revenue-generating.

Pricing tiers

ModelBillingPrice
Other—GPO / negotiated hospital pricing via Premier agreement

Go-to-market motion1 record

Distribution channels5 records

Marketing channels8 records

Cordis product offering

Product offering

Core offering

Cordis manufactures and sells a portfolio of interventional cardiovascular medical devices used by hospitals and physicians for the diagnosis and treatment of coronary and peripheral vascular disease. Its commercial offering spans drug-eluting balloons (SELUTION SLR PTCA and PTA platforms), vascular closure devices (MYNX CONTROL, MYNXGRIP, EXOSEAL), self-expanding and balloon-expandable stents (S.M.A.R.T. RADIANZ, INCRAFT AAA, PALMAZ BLUE, PRECISE), guidewires, diagnostic and guiding catheters, PTA dilatation catheters, embolic protection devices and transradial introducer sheaths. Cordis sells these devices to hospitals and healthcare systems in more than 70 countries through its own direct sales organizations in the Americas, EMEA and APAC.

Product overview

Cordis offers a platform-plus-modules architecture spanning interventional cardiology and peripheral/endovascular interventions, organized across two main portfolios: (1) Interventional Cardiology, anchored by the SELUTION SLR PTCA Drug Eluting Balloon (DEB) using proprietary MicroReservoir sustained sirolimus release, supplemented by MYNX CONTROL / MYNXGRIP / EXOSEAL vascular closure devices, RAIN Sheath transradial introducers, and a full range of guidewires, diagnostic and guiding catheters, and PTCA balloons; and (2) Peripheral Interventions, anchored by the SELUTION SLR PTA Drug Eluting Balloon, the S.M.A.R.T. RADIANZ self-expanding peripheral stent, the BRITE TIP RADIANZ guiding sheath and SABERX RADIANZ PTA dilatation catheter (collectively marketed as the Radianz Radial Peripheral System), the INCRAFT AAA Stent Graft System, the OPTEASE Retrievable Vena Cava Filter, and a full lower-extremity, renal, carotid, and venous portfolio of catheter sheaths, guidewires, diagnostic catheters, and PTA balloons. Cross-cutting products include the ANGIOGUARD RX emboli protection guidewire and the OUTBACK Elite Re-Entry Catheter. Cordis-X serves as an independent innovation accelerator (in partnership with Ajax Health) sourcing new technologies such as the Ladera Large Bore Closure System. Cordis's historical leadership position is rooted in introducing the first guidewire, the first drug-eluting stent (CYPHER), and now the SELUTION SLR DEB platform following the October 2023 MedAlliance acquisition.

Differentiator

Problem solved

Functional benefit

Brands

  • Cordis-X: Independent innovation accelerator / growth engine for Cordis, focused on identifying, investing in, and developing next-generation medical device technologies for the Cordis portfolio.
  • SELUTION SLR™
  • Radianz Radial Peripheral System™
  • MYNX CONTROL™

Products and services

  • SELUTION SLR PTCA Drug Eluting Balloon (DEB) Latest-generation sirolimus drug-eluting balloon for coronary interventions, using proprietary Cell Adherent Technology (CAT) and MicroReservoirs made from biodegradable polymer mixed with sirolimus to provide controlled and sustained drug release for up to 90 days, designed to deliver drug-eluting stent-equivalent performance without leaving a permanent metal implant.
  • SELUTION SLR PTA Drug Eluting Balloon Sirolimus drug-eluting balloon for peripheral (lower extremity / popliteal / SFA) interventions leveraging the MicroReservoir sustained-release technology. Used in the SELUTION SFA Japan Trial and SUCCESS PTA Study demonstrating up to 81.5% 3-year primary patency.
  • RAIN Sheath Transradial Hydrophilic Thin-walled Introducer

Companies that use Cordis

Customer profile

Named customers7 records

Segments4 records

Ideal customer profiles2 records

Cordis technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature7 records

Cordis partnerships and signals

Strategic signal

Partnerships

Eight partnerships are on record, tiered strategic public-sector partner, product innovation partnership, background executive affiliation, strategic cybersecurity vendor, u.s. gpo distribution partnership, flagship acquisition / transformational, growth / venous thromboembolism market expansion and flagship / innovation engine partner.

  • State of Floridastrategic public-sector partnerOthers · 17 March 2026
  • Ladera Medicalproduct innovation partnershipStrategic or Co-development Partner · 23 October 2025Partnership between Cordis-X and Ladera Medical to develop the Ladera Large Bore Closure System, designed for quick, safe vascular closure after percutaneous catheterization. The FASTEN trial has enrolled its first 25 patients with the goal of obtaining CE Mark approval.
  • Cardiovascular Systems, Inc. (CSI)background executive affiliationOthers · 1 April 2025Matthew Muscari, Cordis President of the Americas, previously led CSI's Peripheral Vascular Commercial organization before joining Cordis; not an active commercial partnership but reflects sector expertise and alumni network.
  • Palo Alto Networksstrategic cybersecurity vendorTechnology or Integration · 14 October 2024Cordis partnered with Palo Alto Networks to deploy a cyber transformation initiative protecting patient data and blocking emerging threats across the enterprise. The collaboration was featured as a customer case study.
  • Premier Inc.u.s. gpo distribution partnershipChannel Partner/ Reseller/ Distributor · 18 July 2024Cordis signed a pricing deal with Premier, a major U.S. healthcare group purchasing organization, simultaneously with FDA approval of the MYNX CONTROL Venous Vascular Closure Device. The agreement enables Premier's member hospitals to access Cordis products under negotiated pricing.
  • MedAllianceflagship acquisition / transformationalStrategic or Co-development Partner · 2 October 2023Cordis completed the acquisition of Switzerland-based MedAlliance in October 2023 for up to $1.135 billion including milestone payments through 2029 (initial $35M investment, $200M closing payment, up to $125M regulatory milestones, up to $775M commercial milestones). MedAlliance's proprietary SELUTION SLR™ drug-eluting balloon technology is now central to Cordis's coronary and peripheral vascular portfolios, with over 40,000 SELUTION units used in patient treatment to date.
  • Endovascular Engineering (E2)growth / venous thromboembolism market expansionStrategic or Co-development Partner · 5 April 2022Cordis made a strategic investment in Endovascular Engineering (E2), a Menlo Park-based developer of next-generation thrombectomy devices for Deep Vein Thrombosis (DVT) and Pulmonary Embolism (PE). The investment expands Cordis's portfolio into the Venous Thromboembolism Market. E2 was founded in 2019 by Dr. Luis Savastano and is also backed by Santé Ventures and another strategic investor.
  • Ajax Healthflagship / innovation engine partnerStrategic or Co-development Partner · 1 January 2021Ajax Health partnered with Cordis to lead and fund Cordis-X, Cordis's independent innovation accelerator. Ajax has over 20 years of experience developing medical devices, and Ajax-developed technologies have generated over $750 million in annual revenue for their acquirers and have been used to treat over one million patients. Ajax's CEO Duke Rohlen also serves as CEO of Cordis-X.

Scale indicators12 records

Recent moves9 records

Expansion highlights7 records

Cordis competitors and assessment

Company assessment

Broad incumbents

  • Boston Scientific: Global medical device leader with deep interventional cardiology and peripheral vascular portfolios including drug-eluting stents, balloons, and closure devices. Direct competitor to Cordis in DES, DEB, and vascular closure; serves the same hospitals and interventional cardiologists but at much larger scale.
  • Medtronic: Largest medical device company globally, with leading coronary stent (Resolute Onyx), drug-eluting balloon, and peripheral vascular franchises. Competes head-to-head with Cordis across PCI, peripheral, and AAA stent graft markets through its direct sales force and broad hospital contracts.
  • Abbott: Major cardiovascular device player with Xience DES, peripheral intervention, and structural heart franchises. Competes with Cordis in coronary stents, imaging, and vascular closure through its large direct sales organization and global hospital footprint.
  • Becton Dickinson (BD): BD's Interventional segment (formerly Bard) includes peripheral stents, PTA balloons, drug-coated balloons, and vascular closure devices, directly overlapping Cordis's SFA, BTK, and closure device portfolios. BD's scale and GPO relationships make it one of Cordis's most direct incumbents.

Direct peers

  • Terumo: Japanese medical device company with significant interventional cardiology and vascular closure offerings (e.g., TR Band, drug-eluting technologies through Terumo Medical). Competes with Cordis in transradial access sheaths, vascular closure, and coronary intervention products globally.
  • Teleflex: Medical device company with vascular closure (e.g., MANTA large-bore closure), interventional cardiology, and peripheral vascular products. Directly competes with Cordis's MYNX CONTROL closure portfolio, particularly in the large-bore structural heart and endovascular space.

Emerging players

  • Shockwave Medical: Specialist in intravascular lithotripsy (IVL) for calcium modification in coronary and peripheral interventions. Adjacent disruptor to Cordis's peripheral intervention portfolio; was acquired by Johnson & Johnson, raising competitive intensity in the peripheral space.
  • Penumbra: Focused on mechanical thrombectomy and vascular embolization, overlapping with Cordis's E2 investment and broader peripheral/venous portfolio. Competes in the VTE and peripheral arterial thrombectomy segments where Cordis is expanding.
  • Inari Medical: Pure-play venous thromboembolism and venous intervention device company (acquired by Stryker). Overlaps with Cordis's E2 thrombectomy investment and the OPTEASE vena cava filter franchise in the venous intervention market.
  • AngioDynamics: Mid-cap medical device company focused on peripheral vascular disease and venous intervention, with overlapping product lines in PTA balloons, thrombectomy, and venous access. Smaller scale than Cordis but competes in similar hospital accounts for peripheral intervention procedures.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat6 records

Key risks5 records

Key highlights7 records

Customer concentration

Cordis social profiles

Digital presence

Cordis compliance and trust

Trust signal

Compliance4 records

Cordis financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Cordis leadership team

Management profile

Number of profiles

Profiles10 records

Cordis subsidiaries and ownership

Company hierarchy

Subsidiaries3 records

Cordis funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

Cordis M&A and investment

M&A and investment

M&A4 records

Investments2 records

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

Frequently asked questions about Cordis

What does Cordis do?

Cordis manufactures and sells a portfolio of interventional cardiovascular medical devices used by hospitals and physicians for the diagnosis and treatment of coronary and peripheral vascular disease. Its commercial offering spans drug-eluting balloons (SELUTION SLR PTCA and PTA platforms), vascular closure devices (MYNX CONTROL, MYNXGRIP, EXOSEAL), self-expanding and balloon-expandable stents (S.M.A.R.T. RADIANZ, INCRAFT AAA, PALMAZ BLUE, PRECISE), guidewires, diagnostic and guiding catheters, PTA dilatation catheters, embolic protection devices and transradial introducer sheaths. Cordis sells these devices to hospitals and healthcare systems in more than 70 countries through its own direct sales organizations in the Americas, EMEA and APAC.

Is Cordis a public or private company?

Cordis is a private company. It is classified as private equity controlled and is currently operating.

When was Cordis founded?

Cordis was founded in 1959. It employs 1,001 to 5,000 people.

Where is Cordis based?

Cordis is headquartered in Hialeah, United States, in the North America region.

How does Cordis make money?

Two revenue lines are on record. Cardiovascular medical device sales are the primary driver. The others are medical education and grants programs.

Who are Cordis's main competitors?

Broad incumbents on record are Boston Scientific, Medtronic, Abbott and Becton Dickinson (BD). Direct peers are Terumo and Teleflex. Emerging players are Shockwave Medical, Penumbra, Inari Medical and AngioDynamics.

Does Cordis have an API?

No public API is recorded for Cordis.

What industry is Cordis in?

Cordis's product category is Interventional Cardiology & Endovascular Medical Devices. Its primary akta.pro industry code is HLAHAFAA, Coronary Stents & Drug-Eluting Technologies, with a secondary code of HLAHAFAB, Structural Heart Valves (TAVR/SAVR) & Valve Repair. Its NAICS code is 339112 and its SIC code is 3841.

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YourStorySELUTION SLR™ wins historic US FDA nod for in‑stent restenosisThe US FDA approved SELUTION SLR, a sirolimus drug-eluting balloon for in-stent restenosis, the first and only of its kind in the US. The approval follows a trial of over 400 patients and Cordis's $1.135 billion acquisition of MedAlliance. A second US trial for de novo lesions is underway.Business News TodayNo more metal: World’s first sirolimus drug balloon wins landmark US FDA approval- Moneycontrol.comThe US FDA approved the SELUTION SLR drug-eluting balloon for treating coronary in-stent restenosis, the first sirolimus-based device cleared in the US. The approval followed the SELUTION4ISR trial of over 400 patients, with the balloon used in more than 65 countries for over 250,000 patients. Cordis has completed enrolment in a US trial of 960 patients for a second submission.The TribuneCofounder Amit Bohora Calls It "A Defining Milestone for Stentless Cardiac Care"The U.S. FDA approved SELUTION SLR, a sirolimus drug-eluting balloon for in-stent restenosis, making it the first and only such device in the U.S. Cordis acquired MedAlliance for $1.135 billion in October 2023. The approval follows a trial of over 400 patients and a global evidence base of more than 5,000 patients.Indian Economic ObserverSELUTION SLR™ DEB Wins US FDA Approval for In-Stent Restenosis - Cofounder Amit Bohora Calls It "A Defining Milestone for Stentless Cardiac Care"The U.S. FDA approved SELUTION SLR, a sirolimus drug-eluting balloon for in-stent restenosis, making it the first and only such device in the U.S. The approval follows a trial of over 400 patients and Cordis' $1.135 billion acquisition of MedAlliance in October 2023.MedTech DiveCordis wins FDA approval for sirolimus-eluting balloonCordis received FDA approval for its sirolimus-eluting balloon, Selution SLR, for treating coronary in-stent restenosis. The device is the first sirolimus balloon approved in the U.S., with trial data showing noninferiority to standard care. Cordis has given U.S. physicians immediate access to the product.Medical Device NetworkFDA approves Cordis SELUTION SLR for coronary in-stent restenosisThe FDA approved Cordis' SELUTION SLR drug-eluting balloon for treating coronary in-stent restenosis, giving US physicians immediate access. The device, supported by the SELUTION4ISR trial, showed non-inferiority at 12 months (15.2% vs 13.5% target lesion failure). Cordis is also enrolling patients in a de novo lesion trial.FierceBiotechCordis’ sirolimus drug-coated balloon earns FDA approval as a breakthrough deviceThe FDA approved Cordis' Selution SLR DEB, a sirolimus drug-coated balloon for treating coronary in-stent restenosis. The approval, under the breakthrough device designation, is based on a study of over 400 patients. Cordis also completed enrollment in a 960-patient study for a future pre-market approval.Business Wire BlogSELUTION SLR™ Drug-Eluting Balloon Approved by FDA for In-Stent Restenosis: First and Only Sirolimus Drug-Eluting Balloon in the USCordis announced FDA approval of SELUTION SLR DEB for coronary in-stent restenosis, the first and only sirolimus drug-eluting balloon in the U.S. The SELUTION4ISR trial met its primary endpoint of non-inferiority, with target lesion failure rates of 15.2% for SELUTION SLR and 13.5% for standard of care.FinancialContent Business PageSELUTION SLR™ Drug-Eluting Balloon Approved by FDA for In-Stent Restenosis: First and Only Sirolimus Drug-Eluting Balloon in the USCordis announced FDA approval of SELUTION SLR drug-eluting balloon for coronary in-stent restenosis, the first and only sirolimus DEB in the U.S. The SELUTION4ISR trial met non-inferiority at 12 months, with target lesion failure rates of 15.2% for SELUTION SLR and 13.5% for standard of care.BioSpaceSELUTION SLR™ Drug-Eluting Balloon Approved by FDA for In-Stent Restenosis: First and Only Sirolimus Drug-Eluting Balloon in the USCordis announced FDA approval of SELUTION SLR drug-eluting balloon for coronary in-stent restenosis, the first and only sirolimus DEB in the US. The SELUTION4ISR trial met non-inferiority at 12 months, with target lesion failure rates of 15.2% for SELUTION SLR and 13.5% for standard of care.