Contract
manufacturing

Are you looking for a specialised and reliable partner for the manufacture of patient-specific implants? We also produce patient-specific implants in PEEK and titanium as a legal manufacturer, as well as surgical guides and anatomical models, on behalf of our clients. In doing so, we ensure a controlled and validated manufacturing process for the implants.

When you want to rely on a fully validated environment

Specialised expertise and manufacturing capacity

Setting up and maintaining a manufacturing environment that complies with all applicable laws and regulations is complex and requires specialised knowledge, capacity, and validation.

By making use of our fully equipped and validated facility, you can have your design manufactured in accordance with the relevant standards, without having to establish a complete manufacturing and quality infrastructure yourself. This saves time, capacity, and costs, and enables patient-specific implants to be produced quickly and safely.

Specialised expertise and manufacturing capacity
A clear process, with clearly defined responsibilities

From design to validated manufacturing

Design transfer

You submit your design via our Xilloc Portal. We work with common file formats (STL, STEP, OBJ, Parasolid) and ensure a smooth transfer of the design into our manufacturing process.

Production validation

We assess the design for manufacturability and functional reliability. Where necessary, we work with you to ensure that the design is suitable for manufacture in accordance with the relevant standards.

Manufacturing

Manufacturing takes place within our certified facility, using advanced 3D printing techniques and high-precision machining.

Quality control & release

Each product undergoes extensive quality control before it is released. As the legal manufacturer, we bear responsibility for production and quality assurance.

Xilloc
Xilloc
Xilloc
Xilloc

Manufactured to the highest quality standards

Fully validated in accordance with ISO 13485 and MDR.

Our facility and processes are fully aligned with ISO 13485 and MDR requirements. This enables us to manufacture third-party products and act as the legal manufacturer, with the associated responsibilities for quality and compliance.

Interested in collaborating?

We would be happy to explore the possibilities with you and discuss how we can support manufacturing and quality assurance within your process. Complete the form and we will be in touch promptly.

Frequently asked questions

Contract manufacturing

Yes, you remain fully responsible for the design. We assess the design solely for manufacturability and functional reliability, to ensure that it is suitable for manufacture in accordance with the relevant standards.

We work with common 3D file formats, including STL, STEP, OBJ and Parasolid.

At the start of a collaboration, responsibilities are recorded in an agreement. In short, this means that we act as the legal manufacturer and are responsible for manufacturing and quality assurance. You remain responsible for the design.