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Reprieve Cardiovascular

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uuid000078g

Namestring
Reprieve Cardiovascular
Legal namestring
Reprieve Cardiovascular, Inc.
Company typeenum
Private
Founded yearint
2019
Descriptiontext

Reprieve Cardiovascular is a privately held, clinical-stage medical device company developing the Reprieve System, an Intelligent Decongestion Management (IDM) platform for treating Acute Decompensated Heart Failure (ADHF). The system combines continuous real-time urine output monitoring with a proprietary personalized diuretic dose-finding algorithm and titrated saline replacement, aiming to safely accelerate fluid removal while protecting renal function in patients hospitalized with fluid volume overload. The company is targeting the global ADHF population, including over 6.7 million Americans living with heart failure and over 1 million US ADHF hospitalizations annually, where traditional diuretic therapy — unchanged in approach for roughly 60 years — yields average hospital stays of more than five days and 30-day readmission rates of 20-25%.

The Reprieve System is currently investigational only and not commercially available in either the US or the EU; FDA Investigational Device Exemption (IDE) approval was secured in February 2025 for the global FASTR II pivotal trial (up to 400 patients across the US and Europe) following positive FASTR pilot results in 100 randomized patients, published in JACC: Heart Failure. The company has raised approximately $103M in disclosed equity funding (Series A $42M in February 2024 led by Lightstone Ventures and Sante Ventures; Series B $61M in August 2025 led by Deerfield Management) plus additional exempt offerings, and is led by CEO Mark Pacyna (former Medtronic VP & GM of Peripheral Vascular).

Short descriptiontext

Reprieve Cardiovascular is a clinical-stage medical device company developing the Reprieve System, an intelligent decongestion management platform that uses real-time urine output monitoring and personalized diuretic dosing to treat hospitalized acute decompensated heart failure patients.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersMilford, United States
HQ citystring
Milford
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
heart failure treatment, decongestion management devices, cardiovascular medical devices, fluid management systems, intelligent medical devices
NAICS code1 code
  • Electromedical and Electrotherapeutic Apparatus Manufacturing334510
SIC code1 code
  • Orthopedic, Prosthetic & Surgical Appliances & Supplies3842
Product category
Cardiovascular Medical Devices
Social media profiles1 record
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Medical Device Sales
TypeHardware Sales
Description

Reprieve Cardiovascular is developing the Reprieve System, an intelligent decongestion management medical device for treating acute decompensated heart failure. The company is in clinical development stage with the system not yet commercially available. Revenue will be generated from device sales to hospitals upon regulatory approval.

reprievecardio.com
Marketing channels4 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

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

Cost components5 values
Technology or R&D, Personnel, Operations, Marketing or Sales, Infrastructure
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 2 records shown
1Reprieve System
Description

Personalized intelligent decongestion management (IDM) solution for Acute Decompensated Heart Failure patients

+1 more record
Core offering1 text field

Reprieve Cardiovascular is developing the Reprieve System, an investigational intelligent decongestion management (IDM) medical device for treating acute decompensated heart failure (ADHF). The system continuously monitors real-time physiological parameters such as urine output and uses a personalized dose-finding algorithm to optimize diuretic dosing, automate saline replacement, and recommend when to escalate or end therapy. The product is currently investigational-only in the US (no commercial sale permitted) and does not yet bear CE marking in the EU/EEA; commercial distribution will follow FDA premarket approval.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 7 values shown
  • ~2x faster IV diuretic completion (46 hrs with Reprieve vs 88 hrs with ODT, P = 0.014)
+6 more records
Product overview1 text field

Reprieve Cardiovascular offers a single unified product, the Reprieve System, which is an intelligent decongestion management (IDM) medical device for treating Acute Decompensated Heart Failure (ADHF). The system combines real-time physiological monitoring with automated dose optimization to personalize diuretic therapy while maintaining kidney function through saline replacement.

Product and service1 record
1Reprieve System
CategoryCardiovascular medical devices / heart failure treatment devices
Description

A personalized intelligent decongestion management (IDM) medical device for treating Acute Decompensated Heart Failure (ADHF) patients in the hospital setting. The system continuously monitors real-time physiological parameters such as urine output and uses a personalized dose-finding algorithm to optimize diuretic therapy and titrate saline replacement, enabling physicians to safely accelerate fluid removal, reduce hospital length of stay, and lower readmission rates. It is intended for hospitals and healthcare systems with cardiovascular and heart failure treatment programs.

Scale indicator5 records

Each record includes

Type, Value, Description, Source

Partnership5 partners
Strategic tierKeyTypeStrategic or Co-development PartnerAnnounced on2025-02-11
Description

Dr. James Udelson, Chief of Cardiology and Interim Chief Physician Executive of the CardioVascular Center at Tufts Medical Center, serves as Principal Investigator of the FASTR pilot trial and Chief of the Division of Cardiology. Presented topline results at THT 2025.

Strategic tierKeyTypeStrategic or Co-development PartnerAnnounced on2024-12-16
Description

Dr. Ali Javaheri and team at Washington University School of Medicine enrolled the first patient in the FASTR II pivotal study in August 2025. This represents a key clinical trial partnership for the pivotal study.

Strategic tierKeyTypeStrategic or Co-development PartnerAnnounced on2024-05-02
Description

Reprieve Cardiovascular partnered with Truveta and leading heart failure researchers to analyze real-world heart failure patient data through the TREAT-AHF study. Truveta provides daily updated, regulatory-grade data from over 100 million de-identified patients across 800+ hospitals and 20,000 clinics in the US. This partnership facilitated the TREAT-AHF analysis and publication demonstrating that heart failure decongestion management has not substantially changed in 20 years.

Strategic tierKeyTypeStrategic or Co-development PartnerAnnounced on2024-05-02
Description

Dr. Alexander Sandhu from Stanford University's Division of Cardiovascular Medicine and Stanford Prevention Research Center led the TREAT-AHF study, contributing to understanding contemporary decongestion practices and opportunities to improve patient management paradigm.

Strategic tierKeyTypeStrategic or Co-development PartnerAnnounced on2024-05-02
Description

Dr. Javed Butler, President of Baylor Scott and White Research Institute and Senior Vice President for Baylor Scott and White Health, serves as Global Principal Investigator of the FASTR II pivotal study, providing strategic leadership for the clinical program.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

Large-cap medtech with a substantial heart failure portfolio (including structural heart, critical care monitoring, and heart failure diagnostics). Edwards is the type of strategic acquirer or fast-follower that could compete with or absorb a Reprieve System post-approval, and operates in the same hospital cardiology customer set.

TypeBroad incumbent
Description

Owns the CardioMEMS HF System (implantable pulmonary artery pressure sensor for chronic heart failure management) and a broad cardiovascular device portfolio. Abbott competes for hospital heart failure budget and would be a likely strategic acquirer of a complementary acute-care decongestion platform like Reprieve.

TypeBroad incumbent
Description

Diversified medtech with heart failure diagnostics and monitoring solutions (e.g., LindaCare/remote cardiac diagnostics) and a large hospital sales channel. Reprieve's CEO is a former Medtronic VP&GM, making Medtronic a highly relevant strategic acquirer comparable in customer base and channel.

TypeBroad incumbent
Description

Major cardiovascular device company with heart failure and structural heart franchises and a direct hospital cardiology sales motion. Operates in the same customer segment and would be a comparable strategic acquirer or competitor for hospital heart failure capex budgets.

TypeBroad incumbent
Description

J&J acquired Abiomed (Impella heart pumps) in 2022 to build a heart failure medical device franchise, and Abiomed was an early Reprieve investor. J&J/Abiomed directly addresses acute heart failure in hospitals and is both a natural strategic acquirer and a comparable in the same customer and clinical workflow.

TypeEmerging player
Description

Israel-based developer of an implantable left-atrial pressure sensor (V-LAP) for remote heart failure management. Closest emerging peer in heart failure hemodynamic monitoring/dosing technology targeting a similar cardiometabolic disease space as Reprieve.

7FIRE1
TypeEmerging player
Description

Ireland-based medtech developing an implantable sensor for remote heart failure management. Comparable as an early-stage heart failure monitoring/dosing platform competing for hospital and cardiology mindshare with Reprieve's intelligent decongestion concept.

TypeEmerging player
Description

Houston-based developer of Aortix, a catheter-deployed heart pump for acute decompensated heart failure and cardiogenic shock. Targets the same ADHF patient population as Reprieve but with a mechanical circulatory support rather than fluid-management approach.

TypeEmerging player
Description

France-based developer of a next-generation LVAD using a wave-membrane pump for advanced heart failure. Targets a downstream heart failure population and competes for the same cardiology/cardiothoracic surgery customer set as Reprieve's hospital channel.

TypeEmerging player
Description

San Francisco-based developer of a connected cardiac biomarker scale for non-invasive heart failure monitoring. Adjacent emerging peer in smart, algorithm-driven heart failure management technology addressing similar value-based-care readmission drivers.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat5 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

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
Yes
API detail
Has APIbool
No

Docs URL, Description

AI capability3 records

Each record includes

Type, Description, Source

AI maturity
App detail

Has app

Feature4 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles12 records

Each record includes

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

No data
Compliance1 record

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds8 records

Each record includes

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

Investors9 records

Each record includes

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

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

M&A

Each record includes

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

Investment

Each record includes

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

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

Reprieve Cardiovascular

Cardiovascular Medical Devicesreprievecardio.com

Reprieve Cardiovascular is a clinical-stage medical device company developing the Reprieve System, an intelligent decongestion management platform that uses real-time urine output monitoring and personalized diuretic dosing to treat hospitalized acute decompensated heart failure patients.

What Reprieve Cardiovascular does

Reprieve Cardiovascular is a privately held, clinical-stage medical device company developing the Reprieve System, an Intelligent Decongestion Management (IDM) platform for treating Acute Decompensated Heart Failure (ADHF). The system combines continuous real-time urine output monitoring with a proprietary personalized diuretic dose-finding algorithm and titrated saline replacement, aiming to safely accelerate fluid removal while protecting renal function in patients hospitalized with fluid volume overload. The company is targeting the global ADHF population, including over 6.7 million Americans living with heart failure and over 1 million US ADHF hospitalizations annually, where traditional diuretic therapy — unchanged in approach for roughly 60 years — yields average hospital stays of more than five days and 30-day readmission rates of 20-25%.

The Reprieve System is currently investigational only and not commercially available in either the US or the EU; FDA Investigational Device Exemption (IDE) approval was secured in February 2025 for the global FASTR II pivotal trial (up to 400 patients across the US and Europe) following positive FASTR pilot results in 100 randomized patients, published in JACC: Heart Failure. The company has raised approximately $103M in disclosed equity funding (Series A $42M in February 2024 led by Lightstone Ventures and Sante Ventures; Series B $61M in August 2025 led by Deerfield Management) plus additional exempt offerings, and is led by CEO Mark Pacyna (former Medtronic VP & GM of Peripheral Vascular).

Reprieve Cardiovascular firmographics

Firmographics
Name
Reprieve Cardiovascular
Legal name
Reprieve Cardiovascular, Inc.
Website
https://reprievecardio.com
Company type
Private
Founded year
2019
Operating status
Operating
Headcount range
11–50 employees
Short description
Reprieve Cardiovascular is a clinical-stage medical device company developing the Reprieve System, an intelligent decongestion management platform that uses real-time urine output monitoring and personalized diuretic dosing to treat hospitalized acute decompensated heart failure patients.
Ownership category
akta.pro rank

Where Reprieve Cardiovascular is headquartered

Location

Headquarters

HQ city
Milford
HQ country
United States
HQ region
North America

Offices1 record

Markets served

Reprieve Cardiovascular business model

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

Revenue model

  1. Medical Device Sales: Reprieve Cardiovascular is developing the Reprieve System, an intelligent decongestion management medical device for treating acute decompensated heart failure. The company is in clinical development stage with the system not yet commercially available. Revenue will be generated from device sales to hospitals upon regulatory approval.

Go-to-market motion1 record

Distribution channels1 record

Marketing channels4 records

Reprieve Cardiovascular product offering

Product offering

Core offering

Reprieve Cardiovascular is developing the Reprieve System, an investigational intelligent decongestion management (IDM) medical device for treating acute decompensated heart failure (ADHF). The system continuously monitors real-time physiological parameters such as urine output and uses a personalized dose-finding algorithm to optimize diuretic dosing, automate saline replacement, and recommend when to escalate or end therapy. The product is currently investigational-only in the US (no commercial sale permitted) and does not yet bear CE marking in the EU/EEA; commercial distribution will follow FDA premarket approval.

Product overview

Reprieve Cardiovascular offers a single unified product, the Reprieve System, which is an intelligent decongestion management (IDM) medical device for treating Acute Decompensated Heart Failure (ADHF). The system combines real-time physiological monitoring with automated dose optimization to personalize diuretic therapy while maintaining kidney function through saline replacement.

Differentiator

Problem solved

Functional benefit

Brands

  • Reprieve System: Personalized intelligent decongestion management (IDM) solution for Acute Decompensated Heart Failure patients
  • Personalized Volume Management System (PVM)

Products and services

  • Reprieve System A personalized intelligent decongestion management (IDM) medical device for treating Acute Decompensated Heart Failure (ADHF) patients in the hospital setting. The system continuously monitors real-time physiological parameters such as urine output and uses a personalized dose-finding algorithm to optimize diuretic therapy and titrate saline replacement, enabling physicians to safely accelerate fluid removal, reduce hospital length of stay, and lower readmission rates. It is intended for hospitals and healthcare systems with cardiovascular and heart failure treatment programs.

Quantifiable outcome

  • ~2x faster IV diuretic completion (46 hrs with Reprieve vs 88 hrs with ODT, P = 0.014)
  • +6 more outcomes

Companies that use Reprieve Cardiovascular

Customer profile

Segments2 records

Ideal customer profiles1 record

Reprieve Cardiovascular technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

AI capability3 records

Feature4 records

Reprieve Cardiovascular partnerships and signals

Strategic signal

Partnerships

Five partnerships are on record, tiered key.

  • Tufts Medical Center (Dr. James Udelson)keyStrategic or Co-development Partner · 11 February 2025Dr. James Udelson, Chief of Cardiology and Interim Chief Physician Executive of the CardioVascular Center at Tufts Medical Center, serves as Principal Investigator of the FASTR pilot trial and Chief of the Division of Cardiology. Presented topline results at THT 2025.
  • Washington University School of Medicine in St. LouiskeyStrategic or Co-development Partner · 16 December 2024Dr. Ali Javaheri and team at Washington University School of Medicine enrolled the first patient in the FASTR II pivotal study in August 2025. This represents a key clinical trial partnership for the pivotal study.
  • TruvetakeyStrategic or Co-development Partner · 2 May 2024Reprieve Cardiovascular partnered with Truveta and leading heart failure researchers to analyze real-world heart failure patient data through the TREAT-AHF study. Truveta provides daily updated, regulatory-grade data from over 100 million de-identified patients across 800+ hospitals and 20,000 clinics in the US. This partnership facilitated the TREAT-AHF analysis and publication demonstrating that heart failure decongestion management has not substantially changed in 20 years.
  • Stanford University (Dr. Alexander Sandhu)keyStrategic or Co-development Partner · 2 May 2024Dr. Alexander Sandhu from Stanford University's Division of Cardiovascular Medicine and Stanford Prevention Research Center led the TREAT-AHF study, contributing to understanding contemporary decongestion practices and opportunities to improve patient management paradigm.
  • Baylor Scott and White Research InstitutekeyStrategic or Co-development Partner · 2 May 2024Dr. Javed Butler, President of Baylor Scott and White Research Institute and Senior Vice President for Baylor Scott and White Health, serves as Global Principal Investigator of the FASTR II pivotal study, providing strategic leadership for the clinical program.

Scale indicators5 records

Recent moves6 records

Expansion highlights5 records

Reprieve Cardiovascular competitors and assessment

Company assessment

Broad incumbents

  • Edwards Lifesciences: Large-cap medtech with a substantial heart failure portfolio (including structural heart, critical care monitoring, and heart failure diagnostics). Edwards is the type of strategic acquirer or fast-follower that could compete with or absorb a Reprieve System post-approval, and operates in the same hospital cardiology customer set.
  • Abbott: Owns the CardioMEMS HF System (implantable pulmonary artery pressure sensor for chronic heart failure management) and a broad cardiovascular device portfolio. Abbott competes for hospital heart failure budget and would be a likely strategic acquirer of a complementary acute-care decongestion platform like Reprieve.
  • Medtronic: Diversified medtech with heart failure diagnostics and monitoring solutions (e.g., LindaCare/remote cardiac diagnostics) and a large hospital sales channel. Reprieve's CEO is a former Medtronic VP&GM, making Medtronic a highly relevant strategic acquirer comparable in customer base and channel.
  • Boston Scientific: Major cardiovascular device company with heart failure and structural heart franchises and a direct hospital cardiology sales motion. Operates in the same customer segment and would be a comparable strategic acquirer or competitor for hospital heart failure capex budgets.
  • Johnson & Johnson (Abiomed): J&J acquired Abiomed (Impella heart pumps) in 2022 to build a heart failure medical device franchise, and Abiomed was an early Reprieve investor. J&J/Abiomed directly addresses acute heart failure in hospitals and is both a natural strategic acquirer and a comparable in the same customer and clinical workflow.

Emerging players

  • Vectorious Medical Technologies: Israel-based developer of an implantable left-atrial pressure sensor (V-LAP) for remote heart failure management. Closest emerging peer in heart failure hemodynamic monitoring/dosing technology targeting a similar cardiometabolic disease space as Reprieve.
  • FIRE1: Ireland-based medtech developing an implantable sensor for remote heart failure management. Comparable as an early-stage heart failure monitoring/dosing platform competing for hospital and cardiology mindshare with Reprieve's intelligent decongestion concept.
  • Procyrion: Houston-based developer of Aortix, a catheter-deployed heart pump for acute decompensated heart failure and cardiogenic shock. Targets the same ADHF patient population as Reprieve but with a mechanical circulatory support rather than fluid-management approach.
  • CorWave: France-based developer of a next-generation LVAD using a wave-membrane pump for advanced heart failure. Targets a downstream heart failure population and competes for the same cardiology/cardiothoracic surgery customer set as Reprieve's hospital channel.
  • Bodyport: San Francisco-based developer of a connected cardiac biomarker scale for non-invasive heart failure monitoring. Adjacent emerging peer in smart, algorithm-driven heart failure management technology addressing similar value-based-care readmission drivers.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat5 records

Key risks6 records

Key highlights7 records

Customer concentration

Reprieve Cardiovascular social profiles

Digital presence

Reprieve Cardiovascular compliance and trust

Trust signal

Compliance1 record

Reprieve Cardiovascular financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Reprieve Cardiovascular leadership team

Management profile

Number of profiles

Profiles12 records

Reprieve Cardiovascular funding detail

Funding detail

Funding overview

Funding rounds8 records

Investors9 records

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

Reprieve Cardiovascular 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 Reprieve Cardiovascular

What does Reprieve Cardiovascular do?

Reprieve Cardiovascular is developing the Reprieve System, an investigational intelligent decongestion management (IDM) medical device for treating acute decompensated heart failure (ADHF). The system continuously monitors real-time physiological parameters such as urine output and uses a personalized dose-finding algorithm to optimize diuretic dosing, automate saline replacement, and recommend when to escalate or end therapy. The product is currently investigational-only in the US (no commercial sale permitted) and does not yet bear CE marking in the EU/EEA; commercial distribution will follow FDA premarket approval.

Is Reprieve Cardiovascular a public or private company?

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

When was Reprieve Cardiovascular founded?

Reprieve Cardiovascular was founded in 2019. It employs 11 to 50 people.

Where is Reprieve Cardiovascular based?

Reprieve Cardiovascular is headquartered in Milford, United States, in the North America region.

How does Reprieve Cardiovascular make money?

One revenue line is on record: medical Device Sales.

Who are Reprieve Cardiovascular's main competitors?

Broad incumbents on record are Edwards Lifesciences, Abbott, Medtronic, Boston Scientific and Johnson & Johnson (Abiomed). Emerging players are Vectorious Medical Technologies, FIRE1, Procyrion, CorWave and Bodyport.

Does Reprieve Cardiovascular have an API?

No public API is recorded for Reprieve Cardiovascular.

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Live signals
Business Wire BlogReprieve Cardiovascular Announces Publication of FASTR Pilot Trial Results in JACC: Heart FailureReprieve Cardiovascular published FASTR pilot trial results in JACC: Heart Failure, showing faster decongestion than optimal diuretic therapy without increased safety risks or kidney function worsening. The trial enrolled 100 patients, and the company is now enrolling in the FASTR II pivotal trial, expected to complete enrollment later this year.Business Wire BlogReprieve Cardiovascular to Present at the 37th Annual Piper Sandler Healthcare ConferenceReprieve Cardiovascular announced that CEO Mark Pacyna will present at the 37th Annual Piper Sandler Healthcare Conference in New York City on December 4, 2025, discussing the company's recent milestones and ongoing pivotal FASTR II clinical trial enrollment. The presentation follows the company's recent $61 million Series B financing and progress toward regulatory approval and commercial readiness for the Reprieve System, an intelligent decongestion therapy for acute decompensated heart failure. The company is leveraging algorithmic guidance and real-time physiological monitoring to personalize diuresis therapy and improve patient outcomes.FinSMEsReprieve Cardiovascular Raises $61M in Series B FinancingReprieve Cardiovascular raised $61M in Series B funding led by Deerfield Management. The company will use the funds to support its FASTR II pivotal clinical trial, which has enrolled its first patient, and new commercial activities.MedTech DiveHeart devices pace medtech’s summer funding flowsVenture capital in medtech surged in Q1 2025, with 11 rounds over $100 million and $4.1 billion total. Heart-device companies Kardium, Field Medical, Reprieve Cardiovascular, and Conformal Medical raised funds for atrial fibrillation and heart failure treatments. Neuromodulation devices also attracted investment.VC News DailyReprieve Cardiovascular Banks $61M in Series BReprieve Cardiovascular, a clinical-stage company developing intelligent decongestion management therapy for acute decompensated heart failure, announced the close of an oversubscribed $61 million Series B financing. The round was led by Deerfield Management with participation from multiple venture firms, combining equity investment with a debt facility. Proceeds will support the global FASTR II pivotal clinical trial, which has already enrolled its first patient, as well as commercial readiness activities.MedTech DiveReprieve Cardiovascular raises $61M; Conformal Medical nets $32M for LAAOReprieve Cardiovascular closed a $61 million Series B financing to fund its pivotal clinical trial for a heart failure fluid management system, aiming to improve decongestion management in patients with acute decompensated heart failure. The trial, known as FASTR II, will enroll up to 400 patients in the U.S. and Europe, comparing the Reprieve system to standard diuretic therapy for clinical effectiveness. In a related funding announcement, Conformal Medical raised $32 million to support its pivotal trial for a left atrial appendage occlusion system designed to reduce stroke risk in patients with atrial fibrillation.citybizReprieve Cardiovascular Secures $61 Million FinancingReprieve Cardiovascular closed an oversubscribed $61 million Series B financing round led by Deerfield Management to support its FASTR II pivotal clinical trial for acute decompensated heart failure. The proceeds will fund the rapid execution of the global study, which has already enrolled its first patient, as well as commercial readiness activities. This capital injection follows successful pilot study results and aims to generate evidence for regulatory approval in the United States.MassDeviceReprieve Cardiovascular raises $61M for heart failure treatment systemReprieve Cardiovascular has closed a $61 million oversubscribed Series B financing round led by Deerfield Management to support its heart failure treatment system. The company plans to use the proceeds to execute its pivotal FASTR II clinical trial and prepare for commercial readiness activities. This funding follows successful results from the earlier FASTR pilot study, with Reprieve aiming to submit for FDA premarket approval based on the upcoming trial data.CardiovascularnewsReprieve Cardiovascular announces funding and trial enrolment milestonesReprieve Cardiovascular closed a US$61 million Series B financing round and enrolled the first patient in its global FASTR II pivotal trial for the Reprieve system. The funding, led by Deerfield Management with participation from several other venture firms, will support the execution of the clinical trial and commercial readiness activities. The trial aims to evaluate the efficacy of the Reprieve system against optimal diuretic therapy in patients hospitalized with acute decompensated heart failure across the USA and Europe.Business Wire BlogReprieve Cardiovascular Secures $61 Million Financing and Enrolls First Patient in Pivotal StudyReprieve Cardiovascular closed an oversubscribed $61 million Series B financing round led by Deerfield Management to support the FASTR II pivotal clinical trial and commercial readiness activities. The company simultaneously announced the enrollment of its first patient in the FASTR II study, which is being conducted by Washington University School of Medicine across the United States and Europe.