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Jupiter Endovascular

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uuid000058u

Namestring
Jupiter Endovascular
Legal namestring
Jupiter Endovascular, Inc.
Websiteurl
jupiterendo.com
Company typeenum
Private
Founded yearint
2024
Descriptiontext

Jupiter Endovascular, Inc. is a privately held medical technology company founded in 2024 and headquartered in Menlo Park, California, spun out of Neptune Medical to develop a new class of catheter-based endovascular procedures. Its core innovation is the proprietary Transforming Fixation (TFX) platform technology, also marketed under the Endoportal Control brand, which enables a single catheter to navigate flexibly through the vasculature and then shift into a rigid, stabilized configuration on demand for precise intervention. The company's lead product, the Vertex Pulmonary Embolectomy System, applies TFX to treat acute intermediate-risk pulmonary embolism, where the device is delivered flexibly through the right heart and locked into a stable position within the pulmonary arteries for controlled thrombectomy. Supporting clinical evidence includes the SPIRARE I first-in-human study (10 patients across Austria and Poland, results presented at TCT 2025) and the SPIRARE II U.S. pivotal trial (123 patients across up to 23 sites in the U.S. and Europe, positive pivotal results presented at EuroPCR 2026).

Jupiter Endovascular has raised approximately $61 million across two venture financings, including a $21 million round in August 2024 led by Sonder Capital at stealth emergence and an oversubscribed Series B exceeding $40 million in October 2025 led again by Sonder Capital with participation from Senvest Management, LB Investment, and an unnamed strategic corporate investor. The company received FDA 510(k) clearance for the Vertex Catheter in September 2025 for the insertion of endovascular devices, while the Vertex Pulmonary Embolectomy System itself remains investigational. The leadership team comprises CEO Carl J. St. Bernard (prior senior roles at Johnson & Johnson Vision, Cordis, GE Healthcare), CFO Fred Ong (former CFO at Sirona Medical and Datavant), CSO Chuck Love, and VPs across product development, regulatory, clinical, operations, and marketing.

The business model is enterprise medical device commercialization through direct hospital sales to tertiary and quaternary cardiovascular centers performing pulmonary embolism thrombectomy, including Pulmonary Embolism Response Teams (PERT). Revenue will derive from sales of the Vertex system as capital equipment alongside associated procedural consumables, with go-to-market executed via a field sales motion supported by clinical evidence and key opinion leader engagement. Jupiter has identified a market opportunity of up to 900,000 U.S. pulmonary embolism patients annually and plans to extend the TFX platform into additional high-need cardiovascular applications beyond pulmonary embolism.

Short descriptiontext

Jupiter Endovascular is a Menlo Park-based medical technology company developing the Transforming Fixation (TFX) catheter platform, with its Vertex Pulmonary Embolectomy System targeting acute pulmonary embolism treatment at tertiary cardiovascular centers across the U.S. and Europe.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
51–100
akta.pro rankint
HeadquartersMenlo Park, United States
HQ citystring
Menlo Park
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
endovascular catheter systems, pulmonary embolism treatment, interventional cardiology devices, thrombectomy catheters, cardiovascular medical devices
Industry1 code
1Thrombectomy, Embolic Protection & Stroke Intervention Devices
CodeHLAHAFAJPrimaryYes
NAICS code2 codes
  • Surgical and Medical Instrument Manufacturing339112
  • Electromedical and Electrotherapeutic Apparatus Manufacturing334510
SIC code1 code
  • Surgical & Medical Instruments & Apparatus3841
Product category
Interventional Cardiovascular Medical Devices
Social media profiles1 record
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Vertex Pulmonary Embolectomy System
TypeHardware Sales
Description

The company is preparing for commercialization of its Vertex catheter system for pulmonary embolism treatment. Revenue will be generated through sales of the Vertex system as capital equipment along with associated procedural consumables to hospitals performing PE thrombectomy procedures.

jupiterendo.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 components6 values
Technology or R&D, Personnel, Operations, Supply Chain, Marketing or Sales, Infrastructure
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

Jupiter Endovascular develops and is preparing to commercialize the Vertex Pulmonary Embolectomy System, a catheter-based device for treating acute pulmonary embolism. The system is built on the company's proprietary Transforming Fixation (TFX) platform technology, which allows catheters to navigate flexibly through the vasculature and then transform into a stabilized state for precise, controlled intervention in the pulmonary arteries. The initial commercial focus is on sales of catheter systems and procedural consumables to hospitals and interventional cardiology centers performing PE thrombectomy procedures.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 9 values shown
  • 39% mean reduction in RV/LV ratio at 48 hours in SPIRARE II trial
+8 more records
Product overview1 text field

Jupiter Endovascular offers a unified product system centered on the Vertex Pulmonary Embolectomy System, built upon its proprietary Transforming Fixation (TFX) platform technology. The TFX platform enables the Vertex catheter to decouple flexible navigation from stable support—allowing the device to navigate flexibly through the right heart and then fix into a stable position in the pulmonary arteries for controlled intervention. The initial product application is for pulmonary embolism treatment, with plans to expand TFX into additional cardiovascular applications.

Product and service2 records
1Vertex Pulmonary Embolectomy System
CategoryInterventional Cardiovascular Medical Devices
Description

A catheter-based system for treating acute pulmonary embolism that leverages Transforming Fixation (TFX) technology to navigate flexibly through the right heart and transform into a stabilized state in the pulmonary arteries for precise, controlled thrombectomy intervention. It is being developed for hospitals and interventional cardiology centers performing pulmonary embolism interventions.

2Vertex Catheter (FDA 510(k) Cleared: TFX Platform Catheter)
CategoryInterventional Cardiovascular Medical Devices
Description

The FDA 510(k) cleared catheter platform incorporating Transforming Fixation (TFX) technology, cleared for insertion of endovascular devices. It serves as the underlying catheter platform for the Vertex Pulmonary Embolectomy System and is sold to hospitals and interventional cardiology centers.

Scale indicator5 records

Each record includes

Type, Value, Description, Source

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Inari Medical is the dedicated PE thrombectomy pure-play with FlowTriever and FlowSaver, targeting the same acute/intermediate-risk PE patient population Jupiter is pursuing with Vertex. Both compete for the same hospital accounts, PERT activations, and procedural economics.

TypeDirect peer
Description

Penumbra's Indigo Aspiration System is a leading catheter-based mechanical thrombectomy platform used for PE, sharing the same interventional cardiology/customer base, aspiration-style procedural workflow, and aspiration catheter category with Jupiter's Vertex system.

TypeDirect peer
Description

AngioDynamics markets the AlphaVac mechanical thrombectomy system for PE, directly overlapping Jupiter's clinical use case, hospital buyer profile, and procedural approach for acute pulmonary embolism.

TypeBroad incumbent
Description

Boston Scientific offers the EKOS ultrasonic accelerated thrombolysis system for PE alongside a broad interventional cardiology portfolio, representing a much larger incumbent that competes for PE procedure volumes, hospital contracts, and KOL mindshare.

TypeBroad incumbent
Description

Stryker acquired Inari Medical in 2023, embedding itself in PE thrombectomy, and operates broadly across neurovascular and vascular intervention. As a large incumbent with deep hospital relationships, it is a key strategic counterpart and potential acquirer of next-generation PE technology.

TypeBroad incumbent
Description

Medtronic has a broad cardiovascular and endovascular portfolio and is a long-standing presence in catheter-based interventions. It represents the type of strategic acquirer that could pursue Jupiter's catheter-stabilization platform if commercial traction is demonstrated.

TypeBroad incumbent
Description

Terumo is a major interventional cardiology and endovascular device manufacturer with extensive catheter and access product lines, competing broadly in the same hospital purchasing categories and serving as a credible strategic acquirer of catheter-based innovation.

TypeEmerging player
Description

Rapid Medical develops actively controllable neurovascular and vascular catheters, sharing thematic overlap with Jupiter's TFX stabilization concept and targeting complex endovascular navigation challenges in adjacent vascular territories.

TypeEmerging player
Description

Surmodics has historically been active in vascular intervention and surface coating technologies for endovascular devices, positioning it as an emerging comparable in the broader peripheral and pulmonary vascular catheter space.

TypeOthers
Description

Neptune Medical is the entity from which Jupiter Endovascular was spun out. It is not a direct competitor but a corporate parent/incubator sharing technology lineage and is relevant for understanding Jupiter's IP heritage and potential ongoing commercial relationship.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat3 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 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

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles10 records

Each record includes

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

No data
Compliance1 record

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds3 records

Each record includes

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

Investors4 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 →

Jupiter Endovascular

Interventional Cardiovascular Medical Devicesjupiterendo.com

Jupiter Endovascular is a Menlo Park-based medical technology company developing the Transforming Fixation (TFX) catheter platform, with its Vertex Pulmonary Embolectomy System targeting acute pulmonary embolism treatment at tertiary cardiovascular centers across the U.S. and Europe.

What Jupiter Endovascular does

Jupiter Endovascular, Inc. is a privately held medical technology company founded in 2024 and headquartered in Menlo Park, California, spun out of Neptune Medical to develop a new class of catheter-based endovascular procedures. Its core innovation is the proprietary Transforming Fixation (TFX) platform technology, also marketed under the Endoportal Control brand, which enables a single catheter to navigate flexibly through the vasculature and then shift into a rigid, stabilized configuration on demand for precise intervention. The company's lead product, the Vertex Pulmonary Embolectomy System, applies TFX to treat acute intermediate-risk pulmonary embolism, where the device is delivered flexibly through the right heart and locked into a stable position within the pulmonary arteries for controlled thrombectomy. Supporting clinical evidence includes the SPIRARE I first-in-human study (10 patients across Austria and Poland, results presented at TCT 2025) and the SPIRARE II U.S. pivotal trial (123 patients across up to 23 sites in the U.S. and Europe, positive pivotal results presented at EuroPCR 2026).

Jupiter Endovascular has raised approximately $61 million across two venture financings, including a $21 million round in August 2024 led by Sonder Capital at stealth emergence and an oversubscribed Series B exceeding $40 million in October 2025 led again by Sonder Capital with participation from Senvest Management, LB Investment, and an unnamed strategic corporate investor. The company received FDA 510(k) clearance for the Vertex Catheter in September 2025 for the insertion of endovascular devices, while the Vertex Pulmonary Embolectomy System itself remains investigational. The leadership team comprises CEO Carl J. St. Bernard (prior senior roles at Johnson & Johnson Vision, Cordis, GE Healthcare), CFO Fred Ong (former CFO at Sirona Medical and Datavant), CSO Chuck Love, and VPs across product development, regulatory, clinical, operations, and marketing.

The business model is enterprise medical device commercialization through direct hospital sales to tertiary and quaternary cardiovascular centers performing pulmonary embolism thrombectomy, including Pulmonary Embolism Response Teams (PERT). Revenue will derive from sales of the Vertex system as capital equipment alongside associated procedural consumables, with go-to-market executed via a field sales motion supported by clinical evidence and key opinion leader engagement. Jupiter has identified a market opportunity of up to 900,000 U.S. pulmonary embolism patients annually and plans to extend the TFX platform into additional high-need cardiovascular applications beyond pulmonary embolism.

Jupiter Endovascular firmographics

Firmographics
Name
Jupiter Endovascular
Legal name
Jupiter Endovascular, Inc.
Website
https://jupiterendo.com
Company type
Private
Founded year
2024
Operating status
Operating
Headcount range
51–100 employees
Short description
Jupiter Endovascular is a Menlo Park-based medical technology company developing the Transforming Fixation (TFX) catheter platform, with its Vertex Pulmonary Embolectomy System targeting acute pulmonary embolism treatment at tertiary cardiovascular centers across the U.S. and Europe.
Ownership category
akta.pro rank

Jupiter Endovascular industry classification

Industry
Product category
Interventional Cardiovascular Medical Devices
NAICS
Surgical and Medical Instrument Manufacturing (339112), Electromedical and Electrotherapeutic Apparatus Manufacturing (334510)
SIC
Surgical & Medical Instruments & Apparatus (3841)
akta.pro primary industry
Thrombectomy, Embolic Protection & Stroke Intervention Devices (HLAHAFAJ)

Keywords

  • Endovascular catheter systems
  • Pulmonary embolism treatment
  • Interventional cardiology devices
  • Thrombectomy catheters
  • Cardiovascular medical devices

Where Jupiter Endovascular is headquartered

Location

Headquarters

HQ city
Menlo Park
HQ country
United States
HQ region
North America

Offices1 record

Markets served

Jupiter Endovascular business model

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

Revenue model

  1. Vertex Pulmonary Embolectomy System: The company is preparing for commercialization of its Vertex catheter system for pulmonary embolism treatment. Revenue will be generated through sales of the Vertex system as capital equipment along with associated procedural consumables to hospitals performing PE thrombectomy procedures.

Go-to-market motion1 record

Distribution channels1 record

Marketing channels4 records

Jupiter Endovascular product offering

Product offering

Core offering

Jupiter Endovascular develops and is preparing to commercialize the Vertex Pulmonary Embolectomy System, a catheter-based device for treating acute pulmonary embolism. The system is built on the company's proprietary Transforming Fixation (TFX) platform technology, which allows catheters to navigate flexibly through the vasculature and then transform into a stabilized state for precise, controlled intervention in the pulmonary arteries. The initial commercial focus is on sales of catheter systems and procedural consumables to hospitals and interventional cardiology centers performing PE thrombectomy procedures.

Product overview

Jupiter Endovascular offers a unified product system centered on the Vertex Pulmonary Embolectomy System, built upon its proprietary Transforming Fixation (TFX) platform technology. The TFX platform enables the Vertex catheter to decouple flexible navigation from stable support—allowing the device to navigate flexibly through the right heart and then fix into a stable position in the pulmonary arteries for controlled intervention. The initial product application is for pulmonary embolism treatment, with plans to expand TFX into additional cardiovascular applications.

Differentiator

Problem solved

Functional benefit

Products and services

  • Vertex Pulmonary Embolectomy System A catheter-based system for treating acute pulmonary embolism that leverages Transforming Fixation (TFX) technology to navigate flexibly through the right heart and transform into a stabilized state in the pulmonary arteries for precise, controlled thrombectomy intervention. It is being developed for hospitals and interventional cardiology centers performing pulmonary embolism interventions.
  • Vertex Catheter (FDA 510(k) Cleared: TFX Platform Catheter) The FDA 510(k) cleared catheter platform incorporating Transforming Fixation (TFX) technology, cleared for insertion of endovascular devices. It serves as the underlying catheter platform for the Vertex Pulmonary Embolectomy System and is sold to hospitals and interventional cardiology centers.

Quantifiable outcome

  • 39% mean reduction in RV/LV ratio at 48 hours in SPIRARE II trial
  • +8 more outcomes

Companies that use Jupiter Endovascular

Customer profile

Named customers6 records

Segments2 records

Ideal customer profiles2 records

Jupiter Endovascular technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature3 records

Jupiter Endovascular partnerships and signals

Strategic signal

Scale indicators5 records

Recent moves6 records

Expansion highlights6 records

Jupiter Endovascular competitors and assessment

Company assessment

Direct peers

  • Inari Medical: Inari Medical is the dedicated PE thrombectomy pure-play with FlowTriever and FlowSaver, targeting the same acute/intermediate-risk PE patient population Jupiter is pursuing with Vertex. Both compete for the same hospital accounts, PERT activations, and procedural economics.
  • Penumbra: Penumbra's Indigo Aspiration System is a leading catheter-based mechanical thrombectomy platform used for PE, sharing the same interventional cardiology/customer base, aspiration-style procedural workflow, and aspiration catheter category with Jupiter's Vertex system.
  • AngioDynamics: AngioDynamics markets the AlphaVac mechanical thrombectomy system for PE, directly overlapping Jupiter's clinical use case, hospital buyer profile, and procedural approach for acute pulmonary embolism.

Broad incumbents

  • Boston Scientific: Boston Scientific offers the EKOS ultrasonic accelerated thrombolysis system for PE alongside a broad interventional cardiology portfolio, representing a much larger incumbent that competes for PE procedure volumes, hospital contracts, and KOL mindshare.
  • Stryker: Stryker acquired Inari Medical in 2023, embedding itself in PE thrombectomy, and operates broadly across neurovascular and vascular intervention. As a large incumbent with deep hospital relationships, it is a key strategic counterpart and potential acquirer of next-generation PE technology.
  • Medtronic: Medtronic has a broad cardiovascular and endovascular portfolio and is a long-standing presence in catheter-based interventions. It represents the type of strategic acquirer that could pursue Jupiter's catheter-stabilization platform if commercial traction is demonstrated.
  • Terumo: Terumo is a major interventional cardiology and endovascular device manufacturer with extensive catheter and access product lines, competing broadly in the same hospital purchasing categories and serving as a credible strategic acquirer of catheter-based innovation.

Emerging players

  • Rapid Medical: Rapid Medical develops actively controllable neurovascular and vascular catheters, sharing thematic overlap with Jupiter's TFX stabilization concept and targeting complex endovascular navigation challenges in adjacent vascular territories.
  • Surmodics: Surmodics has historically been active in vascular intervention and surface coating technologies for endovascular devices, positioning it as an emerging comparable in the broader peripheral and pulmonary vascular catheter space.

Others

  • Neptune Medical: Neptune Medical is the entity from which Jupiter Endovascular was spun out. It is not a direct competitor but a corporate parent/incubator sharing technology lineage and is relevant for understanding Jupiter's IP heritage and potential ongoing commercial relationship.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat3 records

Key risks6 records

Key highlights7 records

Customer concentration

Jupiter Endovascular social profiles

Digital presence

Jupiter Endovascular compliance and trust

Trust signal

Compliance1 record

Jupiter Endovascular financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Jupiter Endovascular leadership team

Management profile

Number of profiles

Profiles10 records

Jupiter Endovascular funding detail

Funding detail

Funding overview

Funding rounds3 records

Investors4 records

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

Jupiter Endovascular 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 Jupiter Endovascular

What does Jupiter Endovascular do?

Jupiter Endovascular develops and is preparing to commercialize the Vertex Pulmonary Embolectomy System, a catheter-based device for treating acute pulmonary embolism. The system is built on the company's proprietary Transforming Fixation (TFX) platform technology, which allows catheters to navigate flexibly through the vasculature and then transform into a stabilized state for precise, controlled intervention in the pulmonary arteries. The initial commercial focus is on sales of catheter systems and procedural consumables to hospitals and interventional cardiology centers performing PE thrombectomy procedures.

Is Jupiter Endovascular a public or private company?

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

When was Jupiter Endovascular founded?

Jupiter Endovascular was founded in 2024. It employs 51 to 100 people.

Where is Jupiter Endovascular based?

Jupiter Endovascular is headquartered in Menlo Park, United States, in the North America region.

How does Jupiter Endovascular make money?

One revenue line is on record: vertex Pulmonary Embolectomy System.

Who are Jupiter Endovascular's main competitors?

Direct peers on record are Inari Medical, Penumbra and AngioDynamics. Broad incumbents are Boston Scientific, Stryker, Medtronic and Terumo. Emerging players are Rapid Medical and Surmodics. Neptune Medical is listed as an others.

Does Jupiter Endovascular have an API?

No public API is recorded for Jupiter Endovascular.

What industry is Jupiter Endovascular in?

Jupiter Endovascular's product category is Interventional Cardiovascular Medical Devices. Its primary akta.pro industry code is HLAHAFAJ, Thrombectomy, Embolic Protection & Stroke Intervention Devices. Its NAICS code is 339112 and its SIC code is 3841.

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Live signals
Medical BuyerJupiter Endovascular names Catalin Toma as CMOJupiter Endovascular appointed interventional cardiologist Catalin Toma as its new Chief Medical Officer to lead global clinical strategy. Dr. Toma brings extensive experience in structural heart and interventional cardiology, having previously served as a co-principal investigator for the company’s Vertex™ Thrombectomy System trials.BioSpaceJupiter Endovascular Appoints Catalin Toma, MD, as Chief Medical OfficerJupiter Endovascular appointed Catalin Toma, MD, as Chief Medical Officer, a global role. Toma brings experience as Director of Interventional Cardiology at UPMC and co-PI for Vertex thrombectomy trials. He expressed enthusiasm for the TFX platform's potential in pulmonary embolism treatment.FinancialContent Business PageJupiter Endovascular Appoints Catalin Toma, MD, as Chief Medical OfficerJupiter Endovascular Inc. appointed Dr. Catalin Toma as its new Chief Medical Officer to lead its global medical strategy and clinical development efforts. Dr. Toma brings extensive experience in interventional cardiology and has previously served as a co-principal investigator for the company's Vertex™ Thrombectomy System trials.Mpo-magJupiter Endovascular Announces Positive Results From SPIRARE II Pivotal TrialJupiter Endovascular announced positive results from its SPIRARE II pivotal trial of the Vertex Pulmonary Embolectomy System in acute intermediate-risk pulmonary embolism. The trial met both primary endpoints, showing a 0.39 mean reduction in RV/LV ratio and a 2.4% major adverse event rate. The company plans post-hoc analyses and sees commercialization opportunities for its TFX platform.Clinical Trials ArenaJupiter Endovascular’s pulmonary embolectomy system hits primary endpoints in trialJupiter Endovascular reported positive pivotal trial results for its Vertex pulmonary embolectomy system in the SPIRARE II trial. The 123-patient study met primary endpoints, achieving a 0.39 mean reduction in the RV/LV ratio at 48 hours and a 2.4% major adverse event rate. The data was presented at EuroPCR 2026.Business Wire BlogJupiter Endovascular Announces Positive Results From SPIRARE II Pivotal Trial at EuroPCR 2026Jupiter Endovascular announced that its SPIRARE II pivotal trial evaluating the Vertex Pulmonary Embolectomy System in patients with acute, intermediate-risk pulmonary embolism met both primary endpoints, demonstrating meaningful heart recovery and clinical safety. The trial enrolled 123 patients across 19 sites in Europe and the U.S., showing a 0.39 mean reduction in RV/LV ratio at 48 hours and a 2.4% major adverse event rate, along with 100% technical success and zero use of adjunctive thrombolytics. The company is moving toward commercialization and plans to apply its TFX platform technology across other complex cardiovascular anatomies.Medical Device NetworkJupiter Endovascular completes SPIRARE II trial enrolment for Vertex systemJupiter Endovascular has completed patient enrolment in the SPIRARE II pivotal clinical trial of its Vertex pulmonary embolectomy system for treating acute, intermediate-risk pulmonary embolism. The trial enrolled 123 patients at 23 sites across the US and Europe, with the final participant enrolled by Henry Ford Hospital interventional cardiologist Vikas Aggarwal. The company plans to present trial results later this year, with the Vertex system designed to address challenges in cardiac strain and vessel access during PE thrombectomy using its transforming fixation technology.JupiterendoTransforming Fixation (TFX) - Jupiter EndovascularThe article reports on the Transforming Fixation (TFX) technology developed by Jupiter Endovascular, which allows catheters to transition from flexible to firm. This innovation aims to improve treatment options for pulmonary embolism, a condition that currently leaves many patients at risk for heart failure. The company is targeting underserved markets in cardiovascular therapies with this new approach.FierceBiotechJupiter Endovascular's Vertex TFX catheter platform study shows positive resultsJupiter Endovascular reported positive results from the SPIRARE I trial of its Vertex TFX catheter platform, which treats acute pulmonary embolism without major adverse events in a 10-patient study. The company recently secured $40 million in Series B funding to further develop and launch the platform, following FDA 510(k) clearance for the system in September.Business Wire BlogJupiter Endovascular Announces Positive Results From SPIRARE I First-in-human Study Presented at TCT 2025Jupiter Endovascular announced positive results from its SPIRARE I first-in-human study of the Vertex Pulmonary Embolectomy System with Transforming Fixation (TFX) technology, presented at TCT 2025. The prospective multicenter European study enrolled 10 patients across sites in Austria and Poland, demonstrating no major adverse events within 48 hours and showing clinically meaningful improvements including a 32% reduction in mean pulmonary artery pressure and a 29% improvement in RV/LV ratio. The company is now advancing to SPIRARE II, a pivotal trial enrolling up to 145 patients at up to 25 sites in the U.S. and Europe.