What does glass microdevice contract development actually involve?
Contract development is not prototyping. It is the structured engineering work that makes a device manufacturable, repeatable, and certifiable, before committing to production tooling or volume investment.
Through our proven vertical integration strategy, we have spent the past decade becoming specialists across a vast range of manufacturing processes. At FEMTOPRINT, we seamlessly combine research, product development, and industrialized manufacturing to create high-impact, meaningful products.
We serve as a strategic one-stop shop for development, manufacturing, testing, and assembly. By integrating Design for Manufacturing (DfM) and Design for Assembly (DfA) from the earliest stages, we eliminate unnecessary margin-on-margin costs and guarantee maximum flexibility, delivering both agile prototyping and cost-efficient microfabrication.
Our customers' competitive edge starts at FEMTOPRINT. Our deep expertise in designing for manufacturing, testing, and assembly provides a critical contribution to the overall success of every project. Whether it involves wafer-level manufacturing, ultrafast laser processing, 3D glass structuring, or complex microsystem integration, we ensure your product is optimized for the market.
What feature sizes and geometries are achievable?
FEMTOPRINT's femtosecond laser platform modifies the glass bulk volumetrically — not just at the surface. This enables true 3D geometries: buried channels, internal cavities, undercuts, stacked microfluidic networks, and through-glass vias, all in a single monolithic piece without bonding or assembly.
Typical specifications achievable in contract development:
These are not theoretical limits, they are process-qualified parameters available from the first prototype run.
Is this service suitable for regulated markets?
Yes. FEMTOPRINT SA is certified ISO 13485:2016 for medical device manufacturing and ISO 9001:2015 for general industrial quality management. Contract development projects targeting regulated applications, active implantable devices, in-vitro diagnostic components, drug delivery systems, are managed under our certified QMS from the first design review through pilot production.
We routinely sign NDAs before the first technical conversation. All project data, CAD files, process recipes, and characterization results are handled under strict confidentiality protocols and never shared outside the project team.
How do you start a contract development project with FEMTOPRINT?
You do not need complete CAD files to begin. A clear problem statement, a sketch, and a set of target specifications are sufficient for a first conversation.
The process: submit a contact request or call our engineering team directly. Within one week of a first technical exchange, you receive a written feasibility assessment and a project proposal covering scope, timeline, and cost structure. The initial consultation is complimentary and covered by NDA from the first exchange.
The fastest projects begin with a customer who has already answered three questions internally: what does the device need to do, what are the critical dimensions, and what is the target market or regulatory context. Everything else we develop together.