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BioVentrix

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uuid0002liz

Namestring
BioVentrix
Legal namestring
BioVentrix, Inc.
Websiteurl
bioventrix.com
Company typeenum
Private
Founded yearint
2003
Descriptiontext

BioVentrix is a privately held, clinical-stage medical device company founded in 2003 that develops minimally invasive therapies for congestive heart failure. The company's lead product, the Revivent System (also known as the Revivent TC System), is a hybrid transcatheter ventricular restoration platform that uses pairs of titanium micro-anchors connected by PEEK tethers to reshape the dilated left ventricle and exclude scarred, non-functioning myocardium in patients with ischemic heart failure and reduced ejection fraction. The Less Invasive Ventricular Enhancement (LIVE) procedure is performed by a Heart Team—a cardiothoracic surgeon placing external anchors through a small chest incision and an interventional cardiologist delivering internal anchors via a catheter through the right ventricle—on a beating heart without cardiopulmonary bypass, and is integrated with Philips Healthcare's HeartNavigator 3.0 image fusion software for intra-operative navigation.

BioVentrix generates revenue through direct hospital sales of its Revivent System hardware, currently commercialized in Europe following CE Mark certification in June 2016 and extended in January 2020. The company has built direct sales infrastructure including a VP of Sales for Europe and VP of U.S. Sales, with active commercialization geographies spanning Germany (via the BioVentrix GmbH subsidiary established in Hilden), the Netherlands, and select Asian markets including China (first commercial case at Xiamen Cardiovascular Hospital in March 2017). U.S. commercial approval is being pursued via the RELIVE pivotal trial, a randomized evaluation of approximately 135 subjects that enrolled its first patient at Saint Luke's Mid America Heart Institute in November 2025. Pricing is not publicly disclosed and is negotiated through hospital procurement and reimbursement channels; Germany's consecutive NUB Status 1/1a designations (renewed for 91 hospitals in 2026) enable participating hospitals to negotiate full reimbursement coverage.

Headquartered in Mansfield, Massachusetts (relocated from San Ramon, California), BioVentrix operates with a small team of 1–10 employees and has treated more than 230 patients globally with LIVE Therapy as of mid-2020, reporting zero deaths and zero complications in its most recent 35 consecutive European cases alongside 30–40% left ventricular volume reduction and 17–34% ejection fraction improvement. The company has raised over $230 million in cumulative disclosed funding since 2009, headlined by a $48.5 million Series A in April 2023 led by Andera Partners. In January 2022 BioVentrix acquired MateraCor, Inc. to add an injectable hydrogel heart failure therapy to its portfolio, and in February 2026 it filed for an IPO on Nasdaq (ticker BVXX) seeking up to $17 million with The Benchmark Company as sole bookrunner.

Short descriptiontext

BioVentrix is a clinical-stage medical device company developing the Revivent System, a minimally invasive cardiac remodeling platform using titanium micro-anchors to exclude scar tissue in ischemic heart failure patients, serving hospitals and Heart Teams in Europe and the US.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1–10
akta.pro rankint
HeadquartersSan Ramon, United States
HQ citystring
San Ramon
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices3 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
minimally invasive cardiac devices, ventricular restoration therapy, heart failure treatment, transcatheter cardiac remodeling, ischemic cardiomyopathy devices
Industry3 codes
1Cardiac Surgery Devices (Cannulas, Clamps, Closure, Grafts)
CodeHLAHAFAHPrimaryYes
2Cardiac Assist & Heart Failure Therapies (Implantables, Neuromodulation)
CodeHLAHAFALPrimaryNo
3Interventional Cardiology (PCI/Structural Heart)
CodeHLAKABABPrimaryNo
NAICS code1 code
  • Electromedical and Electrotherapeutic Apparatus Manufacturing334510
SIC code1 code
  • Surgical & Medical Instruments & Apparatus3841
Product category
Cardiac Medical Devices
Social media profiles2 records
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model2 records
1Medical Device Sales (Revivent System)
TypeHardware Sales
Description

BioVentrix generates revenue through the sale of its Revivent System medical devices, consisting of titanium micro-anchor implants with PEEK tethers. The system is currently commercialized in Europe (CE Mark 2016) and in early commercialization stages. The company filed for a $17 million IPO in February 2026 (Nasdaq: BVXX), indicating preparations for public market capital raise and broader commercialization.

bioventrix.com
2Clinical Trial / Development Services
TypeProfessional Services
Description

Revenue from clinical trial enrollment and study-related activities in the US (RELIVE pivotal trial, previously ALIVE trial).

fiercebiotech.com
Marketing channels6 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels3 records

Each record includes

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

Cost components5 values
Technology or R&D, Personnel, Operations, Marketing or Sales, Supply Chain
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 3 records shown
1Revivent System
Description

A minimally invasive cardiac remodeling system that uses titanium micro-anchors and PEEK tethers to reshape the dilated left ventricle in patients with ischemic heart failure and reduced ejection fraction (HFrEF). Also referred to as the Revivent TC System or Revivent TransCatheter Ventricular Enhancement System.

bioventrix.com
+2 more records
Core offering1 text field

BioVentrix develops and sells the Revivent System (Revivent TC System), a minimally invasive cardiac remodeling device that uses titanium micro-anchor implants and PEEK tethers delivered via a hybrid transcatheter approach to reshape the dilated left ventricle and exclude scarred tissue in ischemic heart failure patients. The system is sold to hospitals and heart failure centers in Europe (CE Mark since 2016) and is under US clinical investigation (RELIVE pivotal trial). The LIVE Therapy (Less Invasive Ventricular Enhancement) procedure is performed by a Heart Team combining cardiothoracic surgery and interventional cardiology on a beating heart without cardiopulmonary bypass.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 6 values shown
  • Left ventricular volume reduction: 30-40% (immediate post-procedure)
+5 more records
Product overview1 text field

BioVentrix is a clinical-stage medical device company developing minimally invasive therapies for heart failure. Its flagship product is the Revivent System (also called Revivent TC System), a catheter-based ventricular enhancement device that uses titanium micro-anchors and PEEK tethers to reshape the dilated left ventricle by excluding scarred tissue, performed via the LIVE (Less Invasive Ventricular Enhancement) procedure. The company acquired MateraCor to add injectable hydrogel therapy to its portfolio. The Revivent System holds CE Mark approval for commercialization in Europe and is undergoing the RELIVE pivotal clinical trial in the United States for FDA premarket approval.

Product and service2 records
1Revivent System (Revivent TC TransCatheter Ventricular Enhancement System)
CategoryCardiac medical device for ischemic heart failure treatment
Description

A minimally invasive cardiac remodeling medical device consisting of titanium micro-anchor implants paired with PEEK tethers, delivered via a hybrid transcatheter approach combining cardiothoracic surgery (external anchor through ~4cm chest incision) and interventional cardiology (internal anchor via catheter through the right ventricle). The anchors are drawn together to exclude scarred non-functioning heart wall, reducing left ventricular volume by 30-40% and reshaping the heart to a more normal geometry. Sold to hospitals and heart failure centers in Europe (commercial) and used in US sites under the RELIVE clinical trial (investigational use only).

2MateraCor Injectable Hydrogel Therapy
CategoryCardiac injectable hydrogel therapy for heart failure
Description

An injectable hydrogel therapeutic technology for treating heart failure, acquired by BioVentrix to expand its portfolio of treatments for left ventricular heart failure and add therapeutic options for heart muscle repair beyond the Revivent System.

Scale indicator9 records

Each record includes

Type, Value, Description, Source

Partnership2 partners
Strategic tierStrategic_ExpansionTypeStrategic or Co-development PartnerAnnounced on2022-01-27
Description

BioVentrix acquired MateraCor, a company developing injectable hydrogel for treating heart failure. The acquisition expanded BioVentrix's portfolio of treatments for left ventricular heart failure and added therapeutic options for heart muscle repair beyond the existing Revivent System. Financial terms were not disclosed.

Strategic tierSupportingTypeTechnology or IntegrationAnnounced on2017-04-17
Description

Technology integration partner providing HeartNavigator 3.0 cath lab fusion software used in image fusion-guided Revivent TC procedures. The software enables pre-acquired CT scan fusion with fluoroscopy for real-time intra-operative navigation and accurate anchor implant location determination.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers9 records
TypeBroad incumbent
Description

Medtronic offers LVADs (HVAD legacy, HeartWare acquisition) and broad cardiac surgery and structural heart portfolios addressing the same refractory HF patient pool as Revivent. Comparable as an incumbent with the Heart Team sales footprint, capital resources, and global reimbursement infrastructure that BioVentrix must eventually match or partner with.

TypeBroad incumbent
Description

Boston Scientific has a growing structural heart franchise (Watchman, ACURATE neo2) and serves the same cardiology and cardiothoracic surgery customers. Comparable as a broad incumbent with overlapping call points and Heart Team relationships that BioVentrix targets.

TypeBroad incumbent
Description

LivaNova has a cardiac surgery portfolio (heart-lung machines, oxygenators, Perceval sutureless valves) and serves the same cardiothoracic surgery customers as BioVentrix's external anchor placement. Comparable as a broad incumbent in cardiac surgery devices with overlapping surgical call points in Heart Team centers.

TypeBroad incumbent
Description

Edwards Lifesciences is the structural heart leader (TAVR/SAVR via SAPIEN platform) and serves the same heart teams and HF-adjacent patient populations as BioVentrix. Its established relationships with cardiac surgeons and interventional cardiologists make it both a competitor for procedural capacity and a potential strategic acquirer of BioVentrix's differentiated technology.

TypeEmerging player
Description

BioCardia is developing cardiac cell therapies (e.g., CardiAMP) for ischemic heart failure, addressing an overlapping HFrEF patient population via a different (biologic) modality. Comparable as a clinical-stage HF therapy company competing for the same refractory post-MI LV scar market that BioVentrix's Revivent addresses.

TypeEmerging player
Description

SynCardia manufactures the temporary Total Artificial Heart (TAH-t) for end-stage biventricular failure patients awaiting transplant. Comparable as a mechanical circulatory support company addressing the same advanced HF continuum that BioVentrix targets, though at a more acute end of the severity spectrum.

TypeDirect peer
Description

Corvia Medical makes the Corvia Atrial Shunt (IASD), an interventional device for heart failure targeting a different HF phenotype (HFpEF). Comparable as a transcatheter structural heart device targeting a refractory HF population underserved by GDMT.

TypeDirect peer
Description

Ancora Heart develops the AccuCinch transcatheter ventricular restoration system, which also reshapes the dilated left ventricle in HFrEF patients via a percutaneous approach. Most directly comparable to BioVentrix in target patient population, mechanism (ventricular reshaping without bypass), and clinical-stage status.

TypeBroad incumbent
Description

Abbott markets HeartMate 3 (the leading LVAD) and a structural heart portfolio including MitraClip and Tendyne. Directly competes for treatment of advanced HF patients and has the commercial scale to either displace or acquire emerging ventricular restoration technologies like Revivent.

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 highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers6 records

Each record includes

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

Segment2 records

Each record includes

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

Ideal customer profile1 record

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
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles16 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 rounds18 records

Each record includes

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

Investors5 records

Each record includes

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

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

M&A1 record

Each record includes

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

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

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

BioVentrix

Cardiac Medical Devicesbioventrix.com

BioVentrix is a clinical-stage medical device company developing the Revivent System, a minimally invasive cardiac remodeling platform using titanium micro-anchors to exclude scar tissue in ischemic heart failure patients, serving hospitals and Heart Teams in Europe and the US.

What BioVentrix does

BioVentrix is a privately held, clinical-stage medical device company founded in 2003 that develops minimally invasive therapies for congestive heart failure. The company's lead product, the Revivent System (also known as the Revivent TC System), is a hybrid transcatheter ventricular restoration platform that uses pairs of titanium micro-anchors connected by PEEK tethers to reshape the dilated left ventricle and exclude scarred, non-functioning myocardium in patients with ischemic heart failure and reduced ejection fraction. The Less Invasive Ventricular Enhancement (LIVE) procedure is performed by a Heart Team—a cardiothoracic surgeon placing external anchors through a small chest incision and an interventional cardiologist delivering internal anchors via a catheter through the right ventricle—on a beating heart without cardiopulmonary bypass, and is integrated with Philips Healthcare's HeartNavigator 3.0 image fusion software for intra-operative navigation.

BioVentrix generates revenue through direct hospital sales of its Revivent System hardware, currently commercialized in Europe following CE Mark certification in June 2016 and extended in January 2020. The company has built direct sales infrastructure including a VP of Sales for Europe and VP of U.S. Sales, with active commercialization geographies spanning Germany (via the BioVentrix GmbH subsidiary established in Hilden), the Netherlands, and select Asian markets including China (first commercial case at Xiamen Cardiovascular Hospital in March 2017). U.S. commercial approval is being pursued via the RELIVE pivotal trial, a randomized evaluation of approximately 135 subjects that enrolled its first patient at Saint Luke's Mid America Heart Institute in November 2025. Pricing is not publicly disclosed and is negotiated through hospital procurement and reimbursement channels; Germany's consecutive NUB Status 1/1a designations (renewed for 91 hospitals in 2026) enable participating hospitals to negotiate full reimbursement coverage.

Headquartered in Mansfield, Massachusetts (relocated from San Ramon, California), BioVentrix operates with a small team of 1–10 employees and has treated more than 230 patients globally with LIVE Therapy as of mid-2020, reporting zero deaths and zero complications in its most recent 35 consecutive European cases alongside 30–40% left ventricular volume reduction and 17–34% ejection fraction improvement. The company has raised over $230 million in cumulative disclosed funding since 2009, headlined by a $48.5 million Series A in April 2023 led by Andera Partners. In January 2022 BioVentrix acquired MateraCor, Inc. to add an injectable hydrogel heart failure therapy to its portfolio, and in February 2026 it filed for an IPO on Nasdaq (ticker BVXX) seeking up to $17 million with The Benchmark Company as sole bookrunner.

BioVentrix firmographics

Firmographics
Name
BioVentrix
Legal name
BioVentrix, Inc.
Website
https://bioventrix.com
Company type
Private
Founded year
2003
Operating status
Operating
Headcount range
1–10 employees
Short description
BioVentrix is a clinical-stage medical device company developing the Revivent System, a minimally invasive cardiac remodeling platform using titanium micro-anchors to exclude scar tissue in ischemic heart failure patients, serving hospitals and Heart Teams in Europe and the US.
Ownership category
akta.pro rank

BioVentrix industry classification

Industry
Product category
Cardiac Medical Devices
NAICS
Electromedical and Electrotherapeutic Apparatus Manufacturing (334510)
SIC
Surgical & Medical Instruments & Apparatus (3841)
akta.pro primary industry
Cardiac Surgery Devices (Cannulas, Clamps, Closure, Grafts) (HLAHAFAH)
akta.pro secondary industries
Cardiac Assist & Heart Failure Therapies (Implantables, Neuromodulation) (HLAHAFAL), Interventional Cardiology (PCI/Structural Heart) (HLAKABAB)

Keywords

  • Minimally invasive cardiac devices
  • Ventricular restoration therapy
  • Heart failure treatment
  • Transcatheter cardiac remodeling
  • Ischemic cardiomyopathy devices

Where BioVentrix is headquartered

Location

Headquarters

HQ city
San Ramon
HQ country
United States
HQ region
North America

Offices3 records

Markets served

BioVentrix business model

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

Revenue model

  1. Medical Device Sales (Revivent System): BioVentrix generates revenue through the sale of its Revivent System medical devices, consisting of titanium micro-anchor implants with PEEK tethers. The system is currently commercialized in Europe (CE Mark 2016) and in early commercialization stages. The company filed for a $17 million IPO in February 2026 (Nasdaq: BVXX), indicating preparations for public market capital raise and broader commercialization.
  2. Clinical Trial / Development Services: Revenue from clinical trial enrollment and study-related activities in the US (RELIVE pivotal trial, previously ALIVE trial).

Go-to-market motion1 record

Distribution channels3 records

Marketing channels6 records

BioVentrix product offering

Product offering

Core offering

BioVentrix develops and sells the Revivent System (Revivent TC System), a minimally invasive cardiac remodeling device that uses titanium micro-anchor implants and PEEK tethers delivered via a hybrid transcatheter approach to reshape the dilated left ventricle and exclude scarred tissue in ischemic heart failure patients. The system is sold to hospitals and heart failure centers in Europe (CE Mark since 2016) and is under US clinical investigation (RELIVE pivotal trial). The LIVE Therapy (Less Invasive Ventricular Enhancement) procedure is performed by a Heart Team combining cardiothoracic surgery and interventional cardiology on a beating heart without cardiopulmonary bypass.

Product overview

BioVentrix is a clinical-stage medical device company developing minimally invasive therapies for heart failure. Its flagship product is the Revivent System (also called Revivent TC System), a catheter-based ventricular enhancement device that uses titanium micro-anchors and PEEK tethers to reshape the dilated left ventricle by excluding scarred tissue, performed via the LIVE (Less Invasive Ventricular Enhancement) procedure. The company acquired MateraCor to add injectable hydrogel therapy to its portfolio. The Revivent System holds CE Mark approval for commercialization in Europe and is undergoing the RELIVE pivotal clinical trial in the United States for FDA premarket approval.

Differentiator

Problem solved

Functional benefit

Brands

  • Revivent System: A minimally invasive cardiac remodeling system that uses titanium micro-anchors and PEEK tethers to reshape the dilated left ventricle in patients with ischemic heart failure and reduced ejection fraction (HFrEF). Also referred to as the Revivent TC System or Revivent TransCatheter Ventricular Enhancement System.
  • Revivent Therapy
  • LIVE (Less Invasive Ventricular Enhancement)

Products and services

  • Revivent System (Revivent TC TransCatheter Ventricular Enhancement System) A minimally invasive cardiac remodeling medical device consisting of titanium micro-anchor implants paired with PEEK tethers, delivered via a hybrid transcatheter approach combining cardiothoracic surgery (external anchor through ~4cm chest incision) and interventional cardiology (internal anchor via catheter through the right ventricle). The anchors are drawn together to exclude scarred non-functioning heart wall, reducing left ventricular volume by 30-40% and reshaping the heart to a more normal geometry. Sold to hospitals and heart failure centers in Europe (commercial) and used in US sites under the RELIVE clinical trial (investigational use only).
  • MateraCor Injectable Hydrogel Therapy An injectable hydrogel therapeutic technology for treating heart failure, acquired by BioVentrix to expand its portfolio of treatments for left ventricular heart failure and add therapeutic options for heart muscle repair beyond the Revivent System.

Quantifiable outcome

  • Left ventricular volume reduction: 30-40% (immediate post-procedure)
  • +5 more outcomes

Companies that use BioVentrix

Customer profile

Named customers6 records

Segments2 records

Ideal customer profiles1 record

BioVentrix technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature3 records

BioVentrix partnerships and signals

Strategic signal

Partnerships

Two partnerships are on record, tiered strategic_expansion and supporting.

  • MateraCor, Inc.strategic_expansionStrategic or Co-development Partner · 27 January 2022BioVentrix acquired MateraCor, a company developing injectable hydrogel for treating heart failure. The acquisition expanded BioVentrix's portfolio of treatments for left ventricular heart failure and added therapeutic options for heart muscle repair beyond the existing Revivent System. Financial terms were not disclosed.
  • Philips HealthcaresupportingTechnology or Integration · 17 April 2017Technology integration partner providing HeartNavigator 3.0 cath lab fusion software used in image fusion-guided Revivent TC procedures. The software enables pre-acquired CT scan fusion with fluoroscopy for real-time intra-operative navigation and accurate anchor implant location determination.

Scale indicators9 records

Recent moves6 records

Expansion highlights6 records

BioVentrix competitors and assessment

Company assessment

Broad incumbents

  • Medtronic: Medtronic offers LVADs (HVAD legacy, HeartWare acquisition) and broad cardiac surgery and structural heart portfolios addressing the same refractory HF patient pool as Revivent. Comparable as an incumbent with the Heart Team sales footprint, capital resources, and global reimbursement infrastructure that BioVentrix must eventually match or partner with.
  • Boston Scientific: Boston Scientific has a growing structural heart franchise (Watchman, ACURATE neo2) and serves the same cardiology and cardiothoracic surgery customers. Comparable as a broad incumbent with overlapping call points and Heart Team relationships that BioVentrix targets.
  • LivaNova: LivaNova has a cardiac surgery portfolio (heart-lung machines, oxygenators, Perceval sutureless valves) and serves the same cardiothoracic surgery customers as BioVentrix's external anchor placement. Comparable as a broad incumbent in cardiac surgery devices with overlapping surgical call points in Heart Team centers.
  • Edwards Lifesciences: Edwards Lifesciences is the structural heart leader (TAVR/SAVR via SAPIEN platform) and serves the same heart teams and HF-adjacent patient populations as BioVentrix. Its established relationships with cardiac surgeons and interventional cardiologists make it both a competitor for procedural capacity and a potential strategic acquirer of BioVentrix's differentiated technology.
  • Abbott: Abbott markets HeartMate 3 (the leading LVAD) and a structural heart portfolio including MitraClip and Tendyne. Directly competes for treatment of advanced HF patients and has the commercial scale to either displace or acquire emerging ventricular restoration technologies like Revivent.

Emerging players

  • BioCardia: BioCardia is developing cardiac cell therapies (e.g., CardiAMP) for ischemic heart failure, addressing an overlapping HFrEF patient population via a different (biologic) modality. Comparable as a clinical-stage HF therapy company competing for the same refractory post-MI LV scar market that BioVentrix's Revivent addresses.
  • SynCardia Systems: SynCardia manufactures the temporary Total Artificial Heart (TAH-t) for end-stage biventricular failure patients awaiting transplant. Comparable as a mechanical circulatory support company addressing the same advanced HF continuum that BioVentrix targets, though at a more acute end of the severity spectrum.

Direct peers

  • Corvia Medical: Corvia Medical makes the Corvia Atrial Shunt (IASD), an interventional device for heart failure targeting a different HF phenotype (HFpEF). Comparable as a transcatheter structural heart device targeting a refractory HF population underserved by GDMT.
  • Ancora Heart: Ancora Heart develops the AccuCinch transcatheter ventricular restoration system, which also reshapes the dilated left ventricle in HFrEF patients via a percutaneous approach. Most directly comparable to BioVentrix in target patient population, mechanism (ventricular reshaping without bypass), and clinical-stage status.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks6 records

Key highlights7 records

Customer concentration

BioVentrix social profiles

Digital presence

BioVentrix compliance and trust

Trust signal

Compliance3 records

BioVentrix financial estimates

Financial estimate

Revenue estimate

Valuation estimate

BioVentrix leadership team

Management profile

Number of profiles

Profiles16 records

BioVentrix subsidiaries and ownership

Company hierarchy

Subsidiaries1 record

BioVentrix funding detail

Funding detail

Funding overview

Funding rounds18 records

Investors5 records

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

BioVentrix M&A and investment

M&A and investment

M&A1 record

Investments

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

Frequently asked questions about BioVentrix

What does BioVentrix do?

BioVentrix develops and sells the Revivent System (Revivent TC System), a minimally invasive cardiac remodeling device that uses titanium micro-anchor implants and PEEK tethers delivered via a hybrid transcatheter approach to reshape the dilated left ventricle and exclude scarred tissue in ischemic heart failure patients. The system is sold to hospitals and heart failure centers in Europe (CE Mark since 2016) and is under US clinical investigation (RELIVE pivotal trial). The LIVE Therapy (Less Invasive Ventricular Enhancement) procedure is performed by a Heart Team combining cardiothoracic surgery and interventional cardiology on a beating heart without cardiopulmonary bypass.

Is BioVentrix a public or private company?

BioVentrix is a private company. It is classified as venture growth investor backed and is currently operating.

When was BioVentrix founded?

BioVentrix was founded in 2003. It employs 1 to 10 people.

Where is BioVentrix based?

BioVentrix is headquartered in San Ramon, United States, in the North America region.

How does BioVentrix make money?

Two revenue lines are on record. Medical Device Sales (Revivent System) is the primary driver. The others are clinical Trial / Development Services.

Who are BioVentrix's main competitors?

Broad incumbents on record are Medtronic, Boston Scientific, LivaNova, Edwards Lifesciences and Abbott. Emerging players are BioCardia and SynCardia Systems. Direct peers are Corvia Medical and Ancora Heart.

Does BioVentrix have an API?

No public API is recorded for BioVentrix.

What industry is BioVentrix in?

BioVentrix's product category is Cardiac Medical Devices. Its primary akta.pro industry code is HLAHAFAH, Cardiac Surgery Devices (Cannulas, Clamps, Closure, Grafts), with a secondary code of HLAHAFAL, Cardiac Assist & Heart Failure Therapies (Implantables, Neuromodulation). Its NAICS code is 334510 and its SIC code is 3841.

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Live signals
Renaissance CapitalCardiac medical device developer BioVentrix withdraws $17 million IPOBioVentrix, a cardiac device developer, withdrew its planned Nasdaq IPO on October 14, 2026. The company had filed in February 2026 for a $17 million deal, never setting terms, and last updated its prospectus in May.EIN PresswireBioVentrix® Names Carl Byrnes Chief Financial OfficerBioVentrix appointed Carl Byrnes as Chief Financial Officer, bringing over 25 years of finance experience. He will lead capital strategy and investor relations, supporting the company's pivotal RELIVE trial for its Revivent System. The company aims to build a financially strong medical device company.EIN PresswireBioVentrix, Inc. Announces German Reimbursement DesignationBioVentrix, Inc. announced that the German Institute for the Hospital Remuneration System (InEK) has awarded Revivent Therapy NUB Status 1a designation for 2026, the highest priority designation available in Germany. This designation enables 91 German hospitals to negotiate full reimbursement coverage for the Revivent System, a less invasive cardiac therapy for patients with ischemic heart failure and reduced ejection fraction. The company, headquartered in Mansfield, Massachusetts, described this as a key component of its strategy to expand patient access to the therapy across Germany.Renaissance CapitalCardiac medical device developer BioVentrix files for an $17 million IPOBioVentrix, a Mansfield, Massachusetts-based medical device company developing minimally invasive treatments for heart failure, filed on February 12, 2026 with the SEC for an initial public offering seeking to raise up to $17 million. The company's lead product is the Revivent System, designed to restore left ventricular function in heart failure patients using titanium anchors and PEEK tethers through a minimally invasive procedure. BioVentrix, founded in 2003, plans to list on the Nasdaq under the symbol BVXX, with The Benchmark Company serving as sole bookrunner.EIN PresswireFirst Patient Treated with BioVentrix® Revivent System in RELIVE Trial at Saint Luke’s Mid America Heart InstituteBioVentrix, Inc. announced that the first patient has been treated with its Revivent System in the pivotal RELIVE clinical trial at Saint Luke's Mid America Heart Institute in Kansas City, Missouri. The procedure was performed by Dr. Jessica Heimes on a patient with symptomatic ischemic heart failure characterized by left ventricular scarring from a prior heart attack. The RELIVE trial is evaluating the safety and efficacy of the less invasive Revivent System, which has received FDA Breakthrough Therapy Designation, for restoring left ventricular function in heart failure patients with reduced ejection fraction.SecSEC FORM DBioventrix, Inc., a Delaware-registered biotech company headquartered in Mansfield, Massachusetts, filed a Form D notice with the SEC for an exempt offering of securities under Rule 506(b), involving secured convertible promissory notes with a total offering amount of $12,000,000. The filing indicates $6,672,600 had already been sold to 45 investors as of the first sale date of October 10, 2024, with $5,327,400 remaining to be sold and $120,000 in estimated sales commissions paid to broker-dealers. The offering is intended to last beyond one year, with $800,000 of proceeds designated for payments to executive officers and directors including David Richmond, Michael Taglich, Steven Chartier, Mark Ravich, Rishi Puri, and William Abraham.SecSEC FORM DBioventrix, Inc. filed a Form D with the Securities and Exchange Commission to announce an exempt offering of securities under Rule 506(b). The company is raising up to $3,000,000 through the sale of secured convertible promissory notes, with the first sale occurring on March 22, 2024. The filing lists David Richmond as the CEO signing the document on August 28, 2024.SecSEC FORM DBioventrix Inc. filed a Form D with the SEC on March 29, 2024, announcing an exempt offering of secured convertible promissory notes and equity securities totaling $2.4 million. The filing indicates that the first sale of these securities occurred on March 22, 2024, with 20 investors participating in the round. This regulatory submission serves as formal notice of the private capital raise to federal and state authorities.Pulse 2.0BioVentrix Raises $48.5 Million For Developing Less Invasive Therapies On Treating Failing Left VentriclesBioVentrix raised $48.5 million in a Series A round led by Andera Partners to fund its Revivent TC System's PMA submission and expanded access. The company also received FDA approval for an Expanded Access Program after completing its ALIVE study. The funding supports initial preparations for commercial launch.dlvr.itBioVentrix Raises $48.5 Million For Developing Less Invasive Therapies On Treating Failing Left VentriclesBioVentrix announced the completion of a $48.5 million Series A financing round led by Andera Partners to support its Revivent TC System development and commercial launch preparations. The funding follows FDA approval for an Expanded Access Program after the successful enrollment of the pivotal ALIVE study, which evaluated the device's ability to reconstruct dilated left ventricles in heart failure patients.