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Cardiovalve

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uuid0008xya

Namestring
Cardiovalve
Legal namestring
Cardiovalve
Websiteurl
cardiovalve.com
Company typeenum
Private
Founded yearint
2017
Descriptiontext

Cardiovalve is a clinical-stage medical device company developing a transcatheter valve replacement system designed for transfemoral (percutaneous) delivery, enabling treatment of both mitral and tricuspid valve disease without open-heart surgery. The flagship device is engineered with a short profile to minimize left ventricular outflow tract (LVOT) obstruction, a robust anchoring mechanism for secure positioning in the native anatomy, and an enhanced sealing solution to prevent paravalvular leaks — addressing the most common failure modes in transcatheter valve procedures. The system is currently restricted to research use only and is supported by two clinical programs: the TARGET study for transcatheter tricuspid valve replacement (TTVR), which completed enrollment of 150 patients across Europe, the UK, and Canada in October 2025, and the AHEAD trial for transcatheter mitral valve replacement (TMVR), with preliminary data planned for TCT 2025.

The company operates as a wholly-owned subsidiary of Venus Medtech (Hangzhou) MedTech Co., Ltd., a China-based leader in structural heart solutions, and is headquartered in Or Yehuda, Israel. Cardiovalve generated revenue, when it commences, through hardware sales of valve replacement devices to hospitals and cardiac specialty centers via enterprise field sales and direct procurement relationships. The company submitted its CE Mark technical file in November 2025, with commercial launch in Europe projected for 2027. Target end-users are patients with severe tricuspid or mitral valve disease who are high-risk candidates for conventional open-heart surgery, an underserved segment where the transfemoral approach offers faster recovery and lower procedural risk.

Short descriptiontext

Cardiovalve develops a transfemoral transcatheter valve replacement system for both mitral and tricuspid anatomies, targeting high-risk cardiac surgery patients through hospitals and cardiac specialty centers following CE Mark approval.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1–10
akta.pro rankint
HeadquartersOr Yehuda, Israel
HQ citystring
Or Yehuda
HQ countrystring
Israel
HQ regionstring
Middle East
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
transcatheter valve replacement, mitral valve system, tricuspid valve system, transfemoral delivery device, structural heart devices
Industry2 codes
1Structural Heart Valves (TAVR/SAVR) & Valve Repair
CodeHLAHAFABPrimaryYes
2Interventional Cardiology (PCI/Structural Heart)
CodeHLAKABABPrimaryNo
NAICS code1 code
  • Surgical and Medical Instrument Manufacturing339112
SIC code1 code
  • Surgical & Medical Instruments & Apparatus3841
Product category
Structural Heart Medical Devices
Social media profiles1 record
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model2 records
1Transcatheter Valve Devices
TypeHardware Sales
Description

Cardiovalve is developing and preparing to commercialize its transcatheter valve replacement systems (tricuspid and mitral). As a medical device company, revenue will be generated through the sale of valve replacement devices to hospitals and cardiac centers following regulatory approvals.

cardiovalve.com
2Regulatory Milestones
TypeOne Time License
Description

The company is pursuing CE Mark approval in Europe, planning commercial launch in 2027. This regulatory pathway will enable market access across European territories.

biospace.com
Marketing channels3 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

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

Cost components4 values
Technology or R&D, Operations, Personnel, Others
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

Cardiovalve develops a novel transcatheter heart valve replacement system delivered via a transfemoral (catheter-based) approach, engineered to fit both mitral and tricuspid anatomies. The device avoids open-heart surgery and is currently in clinical/regulatory stage, restricted to research use only.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 value
  • 150 patients treated in TARGET study demonstrated effective reduction of tricuspid regurgitation with acceptable safety profile
Product overview1 text field

Cardiovalve offers a novel transcatheter valve replacement system designed for both mitral and tricuspid valve replacement. The flagship Cardiovalve System uses transfemoral delivery to avoid open heart surgery, featuring a short profile to minimize LVOT obstruction risk, a robust anchoring mechanism, and enhanced sealing to prevent paravalvular leaks. The company's product portfolio is supported by two clinical programs: the TARGET Study for Transcatheter Tricuspid Valve Replacement (TTVR) and the AHEAD Trial for Transcatheter Mitral Valve Replacement (TMVR). The system is currently restricted to research use only.

Product and service3 records
1Cardiovalve System
CategoryTranscatheter Heart Valve Device
Description

A novel transcatheter valve replacement system designed for transfemoral delivery, eliminating the need for open heart surgery. It fits both mitral and tricuspid anatomies and features a short profile to minimize ventricular protrusion and LVOT obstruction risk, a robust anchoring mechanism, and enhanced sealing to prevent paravalvular leaks. Intended for patients with valve disease who are high-risk for open-heart surgery.

2Transcatheter Tricuspid Valve Replacement (TTVR)
CategoryTranscatheter Heart Valve Device
Description

The tricuspid application of the Cardiovalve system, evaluated in the TARGET study. Designed for patients with severe tricuspid regurgitation at high risk for open-heart surgery. The TARGET study enrolled 150 patients across Europe, the UK, and Canada, demonstrating effective reduction of tricuspid regurgitation with an acceptable safety profile.

3Transcatheter Mitral Valve Replacement (TMVR)
CategoryTranscatheter Heart Valve Device
Description

The mitral application of the Cardiovalve system, evaluated in the AHEAD trial for future regulatory approval. Targets patients requiring mitral valve replacement who are high-risk for conventional surgery. Preliminary data planned for presentation at TCT 2025.

Scale indicator3 records

Each record includes

Type, Value, Description, Source

Partnership1 partner
Strategic tierCoreTypeStrategic or Co-development Partner
Description

Cardiovalve operates as a subsidiary of Venus Medtech, a leading Chinese medical device company specializing in structural heart disease solutions. Venus Medtech provides strategic support, resources, and infrastructure for Cardiovalve's transcatheter valve development and clinical programs. The relationship enables technology transfer and shared expertise in transcatheter valve technologies.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

Edwards is the dominant structural heart incumbent with the SAPIEN platform for aortic, transcatheter mitral repair (PASCAL), and an active transcatheter tricuspid program. It is the most consequential competitor in transcatheter valve replacement and shares Cardiovalve's transfemoral, catheter-based approach to mitral and tricuspid disease.

TypeBroad incumbent
Description

Medtronic's Intrepid TMVR program is a leading transcatheter mitral valve replacement system in clinical development, directly comparable to Cardiovalve's mitral offering. Medtronic also has structural heart and tricuspid efforts, placing it in head-to-head competition for structural heart procedure share.

TypeBroad incumbent
Description

Abbott's Tendyne is a leading transcatheter mitral valve replacement system targeting the same high-risk mitral regurgitation patient population as Cardiovalve, and Abbott has growing tricuspid ambitions (TriClip for repair). It competes with Cardiovalve for the same hospital customers and procedures.

TypeDirect peer
Description

JenaValve develops transcatheter aortic and mitral valve replacement systems, including transfemoral delivery devices for structural heart disease. As a focused structural heart company with a transcatheter valve portfolio, it is a close analog to Cardiovalve in technology approach and target market.

TypeBroad incumbent
Description

Venus Medtech is Cardiovalve's parent company and China's leading structural heart company, developing transcatheter aortic, mitral, and tricuspid valve replacement systems. It validates the structural heart TAM and provides manufacturing and commercial reach relevant to assessing Cardiovalve's opportunity set.

TypeDirect peer
Description

NeoVasc is developing the Tiara transcatheter mitral valve replacement system for high-risk mitral patients, positioning it as a direct competitor in TMVR. Its clinical-stage status, mitral focus, and North American/European regulatory pathway align closely with Cardiovalve's profile.

TypeDirect peer
Description

Artivion (formerly CryoLife) operates in the structural heart space with surgical heart valves and is expanding into transcatheter technologies. Its heart valve portfolio competes with Cardiovalve in treating valve disease patients and shares the structural heart commercial footprint.

TypeBroad incumbent
Description

Boston Scientific has expanded aggressively into structural heart through acquisitions (e.g., Bolt, Apollo) and Watchman for adjacent structural procedures, competing with Cardiovalve for hospital structural heart budgets and interventional cardiology workflow.

9LuX-Valve (Peijia Medical)
TypeEmerging player
Description

LuX-Valve is a Chinese developer of transcatheter tricuspid valve replacement systems, directly competing with Cardiovalve in the TTVR space. Its early commercial activity in China and emerging European ambition make it a relevant emerging peer for Cardiovalve's planned 2027 European launch.

TypeBroad incumbent
Description

MicroPort's structural heart division develops transcatheter and surgical valve technologies (e.g., Columbus, Vitaflow), making it a comparable structural heart company with a broader portfolio than Cardiovalve and global commercial reach that Cardiovalve could aspire to in Asia.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment2 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

Feature5 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles2 records

Each record includes

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

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds2 records

Each record includes

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

Investors1 record

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 →

Cardiovalve

Structural Heart Medical Devicescardiovalve.com

Cardiovalve develops a transfemoral transcatheter valve replacement system for both mitral and tricuspid anatomies, targeting high-risk cardiac surgery patients through hospitals and cardiac specialty centers following CE Mark approval.

What Cardiovalve does

Cardiovalve is a clinical-stage medical device company developing a transcatheter valve replacement system designed for transfemoral (percutaneous) delivery, enabling treatment of both mitral and tricuspid valve disease without open-heart surgery. The flagship device is engineered with a short profile to minimize left ventricular outflow tract (LVOT) obstruction, a robust anchoring mechanism for secure positioning in the native anatomy, and an enhanced sealing solution to prevent paravalvular leaks — addressing the most common failure modes in transcatheter valve procedures. The system is currently restricted to research use only and is supported by two clinical programs: the TARGET study for transcatheter tricuspid valve replacement (TTVR), which completed enrollment of 150 patients across Europe, the UK, and Canada in October 2025, and the AHEAD trial for transcatheter mitral valve replacement (TMVR), with preliminary data planned for TCT 2025.

The company operates as a wholly-owned subsidiary of Venus Medtech (Hangzhou) MedTech Co., Ltd., a China-based leader in structural heart solutions, and is headquartered in Or Yehuda, Israel. Cardiovalve generated revenue, when it commences, through hardware sales of valve replacement devices to hospitals and cardiac specialty centers via enterprise field sales and direct procurement relationships. The company submitted its CE Mark technical file in November 2025, with commercial launch in Europe projected for 2027. Target end-users are patients with severe tricuspid or mitral valve disease who are high-risk candidates for conventional open-heart surgery, an underserved segment where the transfemoral approach offers faster recovery and lower procedural risk.

Cardiovalve firmographics

Firmographics
Name
Cardiovalve
Legal name
Cardiovalve
Website
https://cardiovalve.com
Company type
Private
Founded year
2017
Operating status
Operating
Headcount range
1–10 employees
Short description
Cardiovalve develops a transfemoral transcatheter valve replacement system for both mitral and tricuspid anatomies, targeting high-risk cardiac surgery patients through hospitals and cardiac specialty centers following CE Mark approval.
Ownership category
akta.pro rank

Cardiovalve industry classification

Industry
Product category
Structural Heart Medical Devices
NAICS
Surgical and Medical Instrument Manufacturing (339112)
SIC
Surgical & Medical Instruments & Apparatus (3841)
akta.pro primary industry
Structural Heart Valves (TAVR/SAVR) & Valve Repair (HLAHAFAB)
akta.pro secondary industry
Interventional Cardiology (PCI/Structural Heart) (HLAKABAB)

Keywords

  • Transcatheter valve replacement
  • Mitral valve system
  • Tricuspid valve system
  • Transfemoral delivery device
  • Structural heart devices

Where Cardiovalve is headquartered

Location

Headquarters

HQ city
Or Yehuda
HQ country
Israel
HQ region
Middle East

Offices1 record

Markets served

Cardiovalve business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Operations, Personnel, Others

Revenue model

  1. Transcatheter Valve Devices: Cardiovalve is developing and preparing to commercialize its transcatheter valve replacement systems (tricuspid and mitral). As a medical device company, revenue will be generated through the sale of valve replacement devices to hospitals and cardiac centers following regulatory approvals.
  2. Regulatory Milestones: The company is pursuing CE Mark approval in Europe, planning commercial launch in 2027. This regulatory pathway will enable market access across European territories.

Go-to-market motion1 record

Distribution channels1 record

Marketing channels3 records

Cardiovalve product offering

Product offering

Core offering

Cardiovalve develops a novel transcatheter heart valve replacement system delivered via a transfemoral (catheter-based) approach, engineered to fit both mitral and tricuspid anatomies. The device avoids open-heart surgery and is currently in clinical/regulatory stage, restricted to research use only.

Product overview

Cardiovalve offers a novel transcatheter valve replacement system designed for both mitral and tricuspid valve replacement. The flagship Cardiovalve System uses transfemoral delivery to avoid open heart surgery, featuring a short profile to minimize LVOT obstruction risk, a robust anchoring mechanism, and enhanced sealing to prevent paravalvular leaks. The company's product portfolio is supported by two clinical programs: the TARGET Study for Transcatheter Tricuspid Valve Replacement (TTVR) and the AHEAD Trial for Transcatheter Mitral Valve Replacement (TMVR). The system is currently restricted to research use only.

Differentiator

Problem solved

Functional benefit

Products and services

  • Cardiovalve System A novel transcatheter valve replacement system designed for transfemoral delivery, eliminating the need for open heart surgery. It fits both mitral and tricuspid anatomies and features a short profile to minimize ventricular protrusion and LVOT obstruction risk, a robust anchoring mechanism, and enhanced sealing to prevent paravalvular leaks. Intended for patients with valve disease who are high-risk for open-heart surgery.
  • Transcatheter Tricuspid Valve Replacement (TTVR) The tricuspid application of the Cardiovalve system, evaluated in the TARGET study. Designed for patients with severe tricuspid regurgitation at high risk for open-heart surgery. The TARGET study enrolled 150 patients across Europe, the UK, and Canada, demonstrating effective reduction of tricuspid regurgitation with an acceptable safety profile.
  • Transcatheter Mitral Valve Replacement (TMVR) The mitral application of the Cardiovalve system, evaluated in the AHEAD trial for future regulatory approval. Targets patients requiring mitral valve replacement who are high-risk for conventional surgery. Preliminary data planned for presentation at TCT 2025.

Quantifiable outcome

  • 150 patients treated in TARGET study demonstrated effective reduction of tricuspid regurgitation with acceptable safety profile

Companies that use Cardiovalve

Customer profile

Segments2 records

Ideal customer profiles2 records

Cardiovalve technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature5 records

Cardiovalve partnerships and signals

Strategic signal

Partnerships

One partnership is on record.

  • Venus MedtechcoreStrategic or Co-development PartnerCardiovalve operates as a subsidiary of Venus Medtech, a leading Chinese medical device company specializing in structural heart disease solutions. Venus Medtech provides strategic support, resources, and infrastructure for Cardiovalve's transcatheter valve development and clinical programs. The relationship enables technology transfer and shared expertise in transcatheter valve technologies.

Scale indicators3 records

Recent moves6 records

Expansion highlights5 records

Cardiovalve competitors and assessment

Company assessment

Broad incumbents

  • Edwards Lifesciences: Edwards is the dominant structural heart incumbent with the SAPIEN platform for aortic, transcatheter mitral repair (PASCAL), and an active transcatheter tricuspid program. It is the most consequential competitor in transcatheter valve replacement and shares Cardiovalve's transfemoral, catheter-based approach to mitral and tricuspid disease.
  • Medtronic: Medtronic's Intrepid TMVR program is a leading transcatheter mitral valve replacement system in clinical development, directly comparable to Cardiovalve's mitral offering. Medtronic also has structural heart and tricuspid efforts, placing it in head-to-head competition for structural heart procedure share.
  • Abbott: Abbott's Tendyne is a leading transcatheter mitral valve replacement system targeting the same high-risk mitral regurgitation patient population as Cardiovalve, and Abbott has growing tricuspid ambitions (TriClip for repair). It competes with Cardiovalve for the same hospital customers and procedures.
  • Venus Medtech: Venus Medtech is Cardiovalve's parent company and China's leading structural heart company, developing transcatheter aortic, mitral, and tricuspid valve replacement systems. It validates the structural heart TAM and provides manufacturing and commercial reach relevant to assessing Cardiovalve's opportunity set.
  • Boston Scientific: Boston Scientific has expanded aggressively into structural heart through acquisitions (e.g., Bolt, Apollo) and Watchman for adjacent structural procedures, competing with Cardiovalve for hospital structural heart budgets and interventional cardiology workflow.
  • MicroPort Scientific: MicroPort's structural heart division develops transcatheter and surgical valve technologies (e.g., Columbus, Vitaflow), making it a comparable structural heart company with a broader portfolio than Cardiovalve and global commercial reach that Cardiovalve could aspire to in Asia.

Direct peers

  • JenaValve Technology: JenaValve develops transcatheter aortic and mitral valve replacement systems, including transfemoral delivery devices for structural heart disease. As a focused structural heart company with a transcatheter valve portfolio, it is a close analog to Cardiovalve in technology approach and target market.
  • NeoVasc: NeoVasc is developing the Tiara transcatheter mitral valve replacement system for high-risk mitral patients, positioning it as a direct competitor in TMVR. Its clinical-stage status, mitral focus, and North American/European regulatory pathway align closely with Cardiovalve's profile.
  • Artivion (CryoLife): Artivion (formerly CryoLife) operates in the structural heart space with surgical heart valves and is expanding into transcatheter technologies. Its heart valve portfolio competes with Cardiovalve in treating valve disease patients and shares the structural heart commercial footprint.

Emerging players

  • LuX-Valve (Peijia Medical): LuX-Valve is a Chinese developer of transcatheter tricuspid valve replacement systems, directly competing with Cardiovalve in the TTVR space. Its early commercial activity in China and emerging European ambition make it a relevant emerging peer for Cardiovalve's planned 2027 European launch.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks6 records

Key highlights6 records

Customer concentration

Cardiovalve social profiles

Digital presence

Cardiovalve financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Cardiovalve leadership team

Management profile

Number of profiles

Profiles2 records

Cardiovalve funding detail

Funding detail

Funding overview

Funding rounds2 records

Investors1 record

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

Cardiovalve M&A and investment

M&A and investment

M&A

Investments

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

Frequently asked questions about Cardiovalve

What does Cardiovalve do?

Cardiovalve develops a novel transcatheter heart valve replacement system delivered via a transfemoral (catheter-based) approach, engineered to fit both mitral and tricuspid anatomies. The device avoids open-heart surgery and is currently in clinical/regulatory stage, restricted to research use only.

Is Cardiovalve a public or private company?

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

When was Cardiovalve founded?

Cardiovalve was founded in 2017. It employs 1 to 10 people.

Where is Cardiovalve based?

Cardiovalve is headquartered in Or Yehuda, Israel, in the Middle East region.

How does Cardiovalve make money?

Two revenue lines are on record. Transcatheter Valve Devices are the primary driver. The others are regulatory Milestones.

Who are Cardiovalve's main competitors?

Broad incumbents on record are Edwards Lifesciences, Medtronic, Abbott, Venus Medtech, Boston Scientific and MicroPort Scientific. Direct peers are JenaValve Technology, NeoVasc and Artivion (CryoLife). LuX-Valve (Peijia Medical) is listed as an emerging player.

Does Cardiovalve have an API?

No public API is recorded for Cardiovalve.

What industry is Cardiovalve in?

Cardiovalve's product category is Structural Heart Medical Devices. Its primary akta.pro industry code is HLAHAFAB, Structural Heart Valves (TAVR/SAVR) & Valve Repair, with a secondary code of HLAKABAB, Interventional Cardiology (PCI/Structural Heart). Its NAICS code is 339112 and its SIC code is 3841.

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Live signals
PR NewswireCardiovalve presenta el expediente CE para su aprobación tras la finalización exitosa del estudio TARGETCardiovalve, a subsidiary of Venus Medtech, has submitted its CE technical file to DEKRA for regulatory approval of its transcatheter tricuspid valve replacement (TTVR) system, following the successful completion of the TARGET clinical study. The TARGET study enrolled 150 patients across 30 centres in Europe, the UK, and Canada, demonstrating that the Cardiovalve system effectively eliminated tricuspid regurgitation in the majority of patients despite 73% presenting with massive or torrential regurgitation at baseline, while maintaining an acceptable safety profile with symptom improvements at 30 days. Venus Medtech expects to launch the TR system commercially in Europe by 2027, pending CE marking certification.PR NewswireCardiovalve reicht nach erfolgreichem Abschluss der TARGET-Studie CE-Antrag zur Zulassung einCardiovalve, a subsidiary of Venus Medtech, has submitted the technical documents for its Transcatheter Tricuspid Valve Replacement system to DEKRA for CE marking, following successful results from the TARGET clinical study involving 150 patients across Europe, the UK, and Canada. The study demonstrated the system's safety and effectiveness in reducing tricuspidal insufficiency and improving patient symptoms within 30 days, with further long-term results pending.PR NewswireCardiovalve dépose un dossier d'approbation CE suite au succès de l'étude TARGETCardiovalve, a subsidiary of Venus Medtech, has submitted its CE technical file to DEKRA for its transcatheter tricuspid valve replacement (TTVR) system, following the successful completion of the TARGET study involving 150 patients across 30 sites in Europe, the UK, and Canada. Interim results showed the device effectively eliminated tricuspid regurgitation in the majority of patients, with an acceptable safety profile and symptom improvement observed 30 days post-procedure. Venus Medtech CEO indicated Cardiovalve is well-positioned to obtain certification and begin commercial deployment of the TR system by 2027.PR NewswireCardiovalve Submits CE File for Approval Following Successful TARGET Study CompletionVenus Medtech subsidiary Cardiovalve has submitted its CE technical file for its transcatheter tricuspid valve replacement (TTVR) system to DEKRA, the European notified body, following successful completion of the TARGET clinical study. The TARGET study enrolled 150 patients across 30 sites in Europe, the UK, and Canada and demonstrated that the Cardiovalve system effectively eliminated tricuspid regurgitation in the majority of patients while maintaining an acceptable safety profile. Venus Medtech CEO stated the company is well-positioned to achieve CE certification and begin commercial rollout of the tricuspid valve system by 2027.PR NewswireCardiovalve Submits CE File for Approval Following Successful TARGET Study CompletionCardiovalve, a subsidiary of Venus Medtech, has submitted its CE technical file for its transcatheter tricuspid valve replacement (TTVR) system to DEKRA, the European notified body, following the successful completion of the TARGET clinical study. The TARGET study enrolled 150 patients across 30 sites in Europe, the UK, and Canada, demonstrating the system's safety and effectiveness in eliminating tricuspid regurgitation despite 73% of patients presenting with massive or torrential TR at baseline. Venus Medtech's CEO indicated the company is well-positioned to achieve CE certification and begin commercial rollout of the TR system by 2027.BioSpaceCardiovalve Submits CE File for Approval Following Successful TARGET Study CompletionVenus Medtech subsidiary Cardiovalve has submitted the CE technical file for its transcatheter tricuspid valve replacement (TTVR) system to DEKRA for European regulatory approval, following successful completion of the TARGET clinical study. The study enrolled 150 patients across 30 sites in Europe, the UK, and Canada, demonstrating that the Cardiovalve system effectively eliminated tricuspid regurgitation in the majority of patients despite 73% presenting with massive or torrential TR at baseline, with an acceptable safety profile and symptomatic improvements by 30 days. Venus Medtech CEO projects CE certification and commercial rollout of the TR system by 2027.BioSpaceCardiovalve Completes TARGET Study Enrollment for CE Registration Study for Tricuspid Valve ReplacementVenus Medtech subsidiary Cardiovalve has completed enrollment of 150 patients in its TARGET study for Transcatheter Tricuspid Valve Replacement, marking a major milestone toward European regulatory approval with CE Mark submission planned for later this year. Pending approval, commercial launch of the Cardiovalve TTVR system in Europe is projected for 2027. The company is also preparing to initiate the AHEAD study to evaluate its mitral valve replacement system for patients with significant mitral regurgitation.PR NewswireCardiovalve schließt die Rekrutierung für die TARGET-Studie zur CE-Zulassung für den Trikuspidalklappenersatz abVenus Medtech (Hangzhou) Inc. announced that its subsidiary Cardiovalve has completed patient enrollment for the TARGET clinical study, involving a total of 150 patients, for its transcatheter tricuspid valve replacement (TTVR) system. The company is now preparing to submit its CE marking application to European regulators later this year, with a planned European market launch targeted for 2027, pending approval. Cardiovalve is also preparing to initiate the AHEAD study to evaluate its mitral valve replacement system for patients with significant mitral regurgitation, supporting a future CE marking application for that device.PR NewswireCardiovalve termine le recrutement pour l'étude TARGET en vue de l'enregistrement du marquage CE pour le remplacement de la valve tricuspideVenus Medtech announced that its subsidiary Cardiovalve has completed patient recruitment for the TARGET clinical study evaluating its transcatheter tricuspid valve replacement (TTVR) system, with 150 patients enrolled. The company is now preparing to submit a CE marking application to European regulators, targeting a commercial launch in Europe in 2027. Cardiovalve also announced plans to launch the AHEAD study to evaluate its mitral valve replacement system for patients with significant mitral regurgitation.PR NewswireCardiovalve completa la inscripción al estudio TARGETCardiovalve, a subsidiary of Venus Medtech (Hangzhou) Inc., announced the completion of patient enrollment in its TARGET study for Transcatheter Tricuspid Valve Replacement (TTVR), with 150 patients enrolled. The milestone advances the company's regulatory submission for European CE mark approval, planned for year-end 2025, with commercial launch of the Cardiovalve TTVR system targeted for 2027. Cardiovalve also announced plans to initiate the AHEAD study for its mitral valve replacement system and will present preliminary mitral regurgitation data at TCT 2025.