Our mission is to transform ideas into compliant, market-ready medical devices — combining expertise, passion, and precision for a better quality of life.
As a Contract Development & Manufacturing Organisation (CDMO), we guide MedTech companies through the full product journey. From industrial design, electronics, prototyping, and process optimisation to regulatory support, cleanroom production, assembly, packaging, and distribution, we provide end-to-end solutions that accelerate time-to-market.
Backed by ISO 13485 certification, our international team of experts ensures safety, quality, and scalability at every stage.
Through a structured yet flexible process, we work closely with you to conceptualise, design and engineer innovative medical devices.
We take care of every step through a fully customizable path to turn your medical device vision into a market-ready solution.
We bring our experience in the medical sector. Our expertise is the result of a long and well-established journey. We’ve always been a benchmark, ensuring deep knowledge and cutting-edge solutions.
From the first design sketch to market launch, we cover the full spectrum of medical devices across all applications, sizes, and complexities.
More than a partner, a long-term ally.
Built on trust, flexibility, and a shared vision, our collaboration grows with you, whether you’re a startup, SME, or global player. Your success is our mission.
Our international team of experts creates an open environment where ideas flow and challenges are faced together to achieve a strong market impact.
“For one of its most innovative and patented devices, Delmont Imaging has been collaborating with Creanova from design to development, industrialisation, and manufacturing. It was not an easy journey, but the result meets our expectations. Creanova has been …”
Pierre Montillot
CEO
“Collaborating with Creanova has been a rewarding experience thanks to their tailored development and manufacturing services that perfectly align with our needs. Their team consistently demonstrates high motivation, dedication, and …”
Dr. Mark Bispinghoff
COO & Co-founder
“Creanova proved to be an outstanding partner throughout the Origo project. Its unique expertise in the design, development, and manufacturing of medical devices played a critical role in driving the project to successful completion. One of the most notable contributions was …”
Cesare Ferrari
Head of Marketing and Business Development
Our mission is to transform ideas into compliant, market-ready medical devices — combining expertise, passion, and precision for a better quality of life.
As a Contract Development & Manufacturing Organization (CDMO), we guide MedTech companies through the full product journey. From industrial design, electronics, prototyping, and process optimization to regulatory support, cleanroom production, assembly, packaging, and distribution, we provide end-to-end solutions that accelerate time-to-market.
Backed by ISO 13485 certification, our international team of experts ensures safety, quality, and scalability at every stage.
Through a structured yet flexible process, we work closely with you to conceptualize, design and engineer innovative medical devices.
We take care of every step through a fully customizable path to turn your medical device vision into a market-ready solution.
“For one of its most innovative and patented devices, Delmont Imaging has been collaborating with Creanova from design to development, industrialisation, and manufacturing. It was not an easy journey, but the result meets our expectations. Creanova has been …”
Pierre Montillot
CEO
“Collaborating with Creanova has been a rewarding experience thanks to their tailored development and manufacturing services that perfectly align with our needs. Their team consistently demonstrates high motivation, dedication, and …”
Dr. Mark Bispinghoff
COO & Co-founder
Creanova proved to be an outstanding partner throughout the Origo project. Its unique expertise in the design, development, and manufacturing of medical devices played a critical role in driving the project to successful completion. One of the most notable contributions was …”
Cesare Ferrari
Head of Marketing and Business Development
Our certification ensures that every contract manufacturing process complies with rigorous quality management system requirements for medical devices.
This translates into fully compliant products, smooth audits, and a safe path to market.
We guarantee that the devices we design and produce are safe, reliable, and compliant with global standards required by the FDA and MDR, reducing non-compliance risks and accelerating regulatory approval.
Creanova partners with MedTech startups for design, development and manufacturing, accelerating their path through EIC-eligible funding.