PrediSurge and the EIC Accelerator: Digital Twins for Aortic Repair

29 September 2026989 words5 min

Aortic aneurysms can be repaired by placing a stent graft inside the artery, a procedure called EVAR; PrediSurge's risk tool targets type 1A endoleaks, leaks at the top of the graft. PrediSurge, a 2017 spin-off of the engineering school Mines Saint-Étienne, builds patient-specific digital twins of the aorta from CT scans and simulates how a chosen graft will sit, so surgeons can pick a size and model before operating.

The European Innovation Council granted €2,500,000 towards Confident, a €9.09 million project that ran from November 2022 to October 2024. According to the CORDIS report, its Endoleak Risk Index received CE marking in October 2023, the technology was used for 300 patients, and it had more than 80 users across 6 countries. In November 2023 PrediSurge closed a €6.5 million Series A led by the Italian fund LIFTT, with the European Investment Bank and the European Commission among the investors. US approval, the report's next step, has not been announced.

€2.50MEIC grant, 28% of a €9.09M project
€6.5MSeries A, November 2023
2,300+Patients simulated, company claim
−€1.98MNet result in 2025

Company file

Legal entity
PrediSurge, SIREN 829 714 203, Saint-Étienne
Founded
3 May 2017, spin-off of Mines Saint-Étienne
Products
iSizing, Endoleak Risk Index, FEVAR simulation, Virtual Lab
Certification
CE Class IIa medical software; ISO 13485 and 27001
Industry partners
Medtronic, Terumo, Stryker, GE HealthCare, per company
Investors
LIFTT, EIB, European Commission, Saint Victor Capital, UI Investissement, Crédit Agricole LHL Capital Innovation
EIC project
Confident, 1 Nov 2022 to 31 Oct 2024, closed

Where PrediSurge Stands Today

PrediSurge's website now claims more than 2,300 patients simulated, more than 390 clinical centres, 14 patents and 30 scientific publications, and lists Medtronic, Terumo, Stryker and GE HealthCare as partners. It sells automated aortic sizing (iSizing), the Endoleak Risk Index and simulations for fenestrated grafts, and a Virtual Lab for device makers. The French register records a capital increase in August 2026, from €45,721 to €76,611, the first since the Series A; no new round has been announced.

The record

From a school lab to 390 clinical centres, by its own count

PrediSurge obtained CE marking for its endoleak prediction tool during the EIC project and raised a Series A with EU investors.

  1. May 2017Company foundedSpin-off of Mines Saint-Étienne
  2. Mar 2022EIC Accelerator cut-offConfident: simulation platform for cardiovascular interventions
  3. Nov 2022EIC project startsAortic and mitral valve simulation€2.50M grant
  4. Oct 2023CE mark for ERIEndoleak Risk Index for Medtronic's Endurant graft
  5. Nov 2023Series ALIFTT lead; EIB and European Commission among investors€6.5M
  6. Oct 2024EIC project ends300 patients treated, 80+ centres, 6 countries
  7. Aug 2026Capital increaseShare capital raised from €45,721 to €76,611

PrediSurge, Mind Health, CORDIS and Pappers.

The Technology: Simulating the Graft Before the Operation

The software builds a mechanical model of the patient's aorta and of the chosen graft and simulates the deployment. The CORDIS report claims "99% spatial accuracy in device positioning" across more than 150 patients in three clinical studies. The Endoleak Risk Index, validated for Medtronic's Endurant graft, estimates the risk of a type 1A leak for different graft sizes; adaptation for Terumo and Gore grafts began during the project. A mitral valve model was also in a 20-patient clinical study, with 2 cases validated by project end.

The uptake

Clinical centres using the platform

The October 2024 figure comes from the EIC project report; the 2026 figure is the company's website claim.

CORDIS project 190115232 report; PrediSurge website, 2026.

What the EIC Project Promised, and What CORDIS Shows

The EIC project

The EU paid 28% of a €9.09M project

Confident ran from November 2022 to October 2024. The award was blended finance.

CORDIS project 190115232. Values in € millions.

Confident promised "the digital simulation platform that revolutionizes cardiovascular interventions". The report shows a CE-marked aortic product, a quality system audited by TÜV SÜD, a patent filing for the risk index, and a planned pilot with Medtronic Europe on retrospective data from 23 patients. The mitral valve work was still early, and FDA approval was listed as future work.

  1. CE-marked aortic toolsDeliveredERI marked October 2023.
  2. Clinical useDelivered300 patients by 2024.
  3. Mitral valve simulationEarly2 of 20 cases validated.
  4. US approvalNot announcedListed as next step.

What Has Happened Since the Award

A study published in PubMed Central reported early clinical experience with the Endoleak Risk Index in planning aortic repairs, supporting its use for individual decisions and training. PrediSurge had raised a first round of €1.5 million in 2020, before the Series A.

The Money

PrediSurge keeps its revenue confidential. The net results recorded by Pappers were losses of €2.53 million in 2023, €0.74 million in 2024 and €1.98 million in 2025, with staff in the 20 to 49 band. The EIC grant covered 28% of the project; CORDIS does not say who funded the remaining €6.6 million or so.

The accounts

Losses, with revenue kept confidential

Net result in millions of euros. PrediSurge does not publish its revenue. Staff was in the 20 to 49 band in 2023 to 2025.

French company register via Pappers.

What cannot be checked

PrediSurge's revenue, how many centres pay for the software rather than use free tools, how much the EU invested in the Series A, and what the 2026 capital increase raised are not public.

Why Europe Should Care

Simulation-based planning is a field where a small French company works with the world's largest device makers. The EIC paid for part of a project that put a certified product on the market in Europe; the company has not announced US approval for its risk tool.

What the project promised

A digital simulation platform that revolutionises cardiovascular interventions.

What the record shows

CE-marked aortic tools, 300 patients by 2024 and 390 centres claimed in 2026, a €6.5M Series A, no FDA approval announced and revenue kept private.

The Verdict

Certified in Europe, still proving itself

According to CORDIS, Confident delivered a CE-marked product in clinical use, and PrediSurge raised money from EU and private investors during the project. Revenue, US approval and the mitral valve work, which would show whether this is a business and not only a tool, are not yet in the public record.

PrediSurge has not been asked for comment for this article. It is based entirely on company statements, French company data, scientific literature and EU project data, linked throughout.

Industry

HealthMedical devices

Focus
  • Cardiovascular devices
Technologies
  • Computational modelling
Keywords
  • Digital twins
  • Aortic aneurysm
  • Endovascular aneurysm repair
  • Surgical planning