Axiles Bionics closes €6M tranche of Series A to scale Lunaris and develop next generation bionic feet

Brussels, June 30th 2025
Summary
  • Axiles Bionics has closed the first €6 million of an intended €8 million Series A to commercialize its Lunaris bionic foot and advance next generation devices.
  • The round is led by PE Group and includes participation from the EIC Fund, Finance&Invest.brussels, entrepreneurs, private investors and company management.
  • Lunaris is CE marked and FDA cleared and the company says clinical adoption is rising, while it pursues a Prosthetics-as-a-Service business model.
  • Axiles is a 2019 spin off from Brubotics at Vrije Universiteit Brussel and is supported by an EIC Accelerator project started in 2023.
  • Key challenges remain for scaling including manufacturing, regulatory diversity, reimbursement and proving long term clinical benefits and cost effectiveness.

Axiles Bionics raises growth capital to commercialize Lunaris and develop next generation smart bionics

Axiles Bionics, a Belgian deeptech medtech spin off from Brubotics at the Vrije Universiteit Brussel, has announced the first closing of a Series A round with €6 million secured out of an intended €8 million. The financing is led by PE Group and supported by the European Innovation Council Fund, Finance&Invest.brussels, entrepreneurs, private investors and company management. Company executives say the capital will accelerate international rollout of Lunaris, the company’s biomimetic ankle foot prosthesis, and fund development of next generation smart bionic mobility solutions.

Who invested and how the round is structured

Axiles reports a mix of institutional and private investors. The EIC Fund participation is notable because it signals EU backing for deeptech in health and robotics. The company says the round remains open to reach a total of €8 million, with the additional funds intended to complete the Series A.

ItemDetails
Series A target€8 million
Closed to date€6 million
Lead investorPE Group
Other participantsEIC Fund, Finance&Invest.brussels, entrepreneurs, private investors, management

What Lunaris is and what the company claims it does

Axiles describes Lunaris as a biomimetic prosthetic foot that combines adaptive mechanical design with embedded intelligence to produce more intuitive and natural gait patterns. According to the company, Lunaris is CE marked and FDA cleared and is being adopted in clinical settings in multiple countries. The firm positions Lunaris as part of a broader shift from passive prosthetic components to active, sensorised, software driven devices that aim to restore lifelike movement for lower limb amputees.

Biomimetic prosthesis:A prosthesis designed to reproduce aspects of natural human ankle foot mechanics. This can include multi axis movement, energy return characteristics and control algorithms that adapt to walking speed and terrain.
Embedded intelligence and adaptive mechanics:Onboard sensors and software that detect user intent and environmental conditions and then adjust mechanical response in real time. The aim is to provide smoother transitions and reduce compensatory movements that commonly occur with passive prostheses.
Regulatory status:Axiles states Lunaris is CE marked and FDA cleared. CE marking indicates conformity with EU medical device regulations. FDA clearance typically refers to 510k clearance which means a device is substantially equivalent to a legally marketed device in the United States. Both credentials are important for market access but they do not guarantee reimbursement or broad clinical adoption.

Business model: Prosthetics as a Service and commercial strategy

The company is promoting a Prosthetics as a Service model, abbreviated PraaS, that aims to reduce upfront costs for users and integrate device updates, maintenance and user support into a subscription or service agreement. Axiles says PraaS can make advanced bionics more accessible. The new funding is earmarked to accelerate international commercialization of Lunaris and to push work on next generation devices that are in advanced development.

Prosthetics as a Service (PraaS):A purchasing model that spreads cost over time and bundles device maintenance, upgrades and support. It can lower entry barriers but requires operational capacity for logistics, clinical partnerships and data management.

Company background, team and recognition

Axiles Bionics was founded in 2019 as a spin off from Brubotics at Vrije Universiteit Brussel. The company has a 15 person multidisciplinary team with more than two thirds of staff employed as engineers. Axiles holds a growing intellectual property portfolio and has been awarded recognitions such as the European Innovation Award and an Innovative Start up Award. The company’s EIC Accelerator project called Solaris began in 2023 and has supported development and scaling activities under Horizon Europe related frameworks.

EIC Accelerator and EIC Fund support:The EIC Accelerator is an EU funding instrument for disruptive innovations. The EIC Fund provides equity investments to help scale companies that have already received EIC grants. Participation by the EIC Fund signals public backing but it is not a commercial guarantee.

Timeline and planned milestones

DateMilestoneNotes
2019Company foundedSpin off from Brubotics at VUB
2023EIC Accelerator Solaris project startsProject support under Horizon Europe related programmes
24 June 2025Axiles press release announcing Series A partial closeFirst €6 million closed of €8 million target
2025 to coming yearsInternational commercialization and next generation developmentCompany states next generation devices will be launched in coming years

Near term outlook and practical challenges

While the Series A tranche and regulatory clearances are important milestones, several non trivial hurdles remain for Axiles and other companies commercialising active prosthetic devices. Manufacturing scale up for mechanically complex and electronically integrated devices is costly. Certification in one jurisdiction does not automatically ease entry into others because regulatory frameworks and reimbursement systems differ by country. Clinical adoption depends on robust evidence of long term functional benefit, durability and cost effectiveness compared with established solutions. Prosthetics as a Service requires a logistics and clinical network to deliver fitting, maintenance and software updates at scale.

Reimbursement and health systems:Securing payment from insurers or public health systems is often decisive for uptake. Advanced devices face scrutiny on price and must show they improve outcomes or reduce other costs to be reimbursed at scale.
Clinical evidence requirement:Early clinical adoption can be driven by specialist centres and patient demand. Widespread adoption typically requires larger scale studies that demonstrate functional improvements, patient reported outcomes and device durability over time.

Why this matters for European deeptech and health innovation

Axiles is an example of a European deeptech medical robotics company that has moved from university lab to market facing product with public and private backing. The involvement of the EIC Fund underlines EU policy intent to support technology driven health innovations and to retain strategic capabilities in robotics and medtech. The next phase will test whether public and private capital, academic roots and small engineering teams can overcome operational and market access barriers to deliver products at scale and at price points that broaden accessibility.

Takeaway

The €6 million tranche provides Axiles with capital to expand Lunaris commercially and to continue developing future devices. The company holds regulatory clearances and early awards but still faces the standard gauntlet for medical devices which includes manufacturing scale up, long term clinical validation, and variable reimbursement across markets. Watching how the company uses the remaining Series A funds and how it demonstrates clinical and economic value will determine whether Lunaris and the PraaS model can move from promising innovation to widely available care option.