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Services / Portfolio

As an engineering office and design service provider based in Munich, we develop complex technical products and devices through to production readiness—from the initial concept, through CAD design and prototyping, to a production-ready solution.

 

Our focus is on mechanical engineering for medical technology, laboratory equipment, mechanical engineering, plastics technology, building services engineering, and environmental technology.

 

Projects start off in various stages, whether it’s just an idea, an initial concept, or an existing design that needs further refinement.

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We use SolidWorks, PTC Creo, Siemens NX, and Autodesk Inventor for design and follow established methods such as Design for Manufacturing (DfM) and Design for Assembly (DfA).

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Key areas of development

Prototyping and risk mitigation

Prototyping and risk mitigation

Prototypes help identify technical risks and critical assumptions early on. Validation is conducted in a targeted manner based on these critical assumptions.

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We develop functional prototypes and prototypes in our own workshop. We test our assumptions from a technical and functional perspective, as well as in the context of actual use. 

 

For prototype construction, we use lathes and milling machines in our workshop, as well as resin and filament 3D printing. We manufacture parts ourselves, assemble and customize parts from our supplier network, and test our functional prototypes specifically against critical requirements such as strength, ergonomics, and handling.

The added value

  • ​Early risk transparency

  • Fact-based technical decisions

  • Avoiding unnecessary loops

  • Speeding up development
     

Product development and system architecture

Product development and system architecture

We develop clear and robust architectures as the foundation for complex products. To do this, we define functions, modules, and interfaces in a structured manner and integrate them into a manageable overall system.

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In doing so, we take into account interfaces with electronics, software, and supplier components, as well as with existing mechanical assemblies, sheet metal structures, housing designs, and kinematic systems.

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We integrate core technologies and existing solutions in a targeted manner. To ensure that everything fits together in the end, we coordinate technical interdependencies and collaborate with development partners and suppliers.

The added value

  • Clear system boundaries

  • Structured product architectures

  • Coordinated development process

  • A scalable basis for variants and further developments
     

Industrialization and readiness for mass production

Industrialization and readiness for mass production

A working prototype is not yet a product ready for mass production. We develop solutions that can be manufactured reliably and cost effectively.

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Cost and quality are integral parts of series development. Throughout the entire development process, we maintain close communication with both your suppliers and ours. We are happy to recommend trusted partners from our network.

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We manage the transition to production for sheet metal parts, plastic parts, and machined parts, including tolerance management, tooling, and process coordination with your manufacturing partners and our supplier network.

We prepare for handover to production in a structured manner. Documentation and decisions remain traceable throughout the process.

The added value

  • Products that can be manufactured cost effectively

  • Smooth start to mass production

  • Seamless handover to production

  • Plannability for scaling

Variant Development

Product Variant Development and Cost Engineering

A successful product does not target every customer segment.

Price-conscious target audiences need the same core features, but not the same range of functions.

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We analyze existing products in terms of their features, costs, and potential for reuse.

Based on this, we develop cost-optimized variants that are specifically tailored to the requirements of the respective customer segment. Essential functions are retained, while non-essential features are consistently eliminated, including those related to manufacturing and assembly.

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The distinction from the premium product is deliberately maintained. This allows our clients to open up additional market segments without diluting their existing product line.

The added value

  • Products that can be manufactured cost effectively

  • Smooth start to mass production

  • Seamless handover to production

  • Plannability for scaling

Controlled and demanding operating environments

Controlled and demanding operating environments

Products must perform under real-world operating conditions.

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These include harsh environments, safety-critical applications, and regulated fields of use.

Use contexts, standards, safety, and long-term operation are key factors influencing the development process from the very beginning. Maintenance and service are also considered as integral parts of the system design.

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For medical technology projects in particular, we incorporate requirements in terms of ISO 13485, IEC 60601, and the EU MDR as early as the concept phase, as well as protection ratings (IP), EMC, and environmental requirements for continuous industrial use.

The added value

  • Opening up additional customer segments

  • Clearly distinct variants instead of cannibalization

  • Reuse of proven assemblies

  • Flexibility for internal product strategy

Tools we use

Our capabilities and tools

  • CAD Design: SolidWorks, PTC Creo, Siemens NX, Autodesk Inventor

  • Simulation: SolidWorks Simulation, Siemens NX (FEM strength analysis)

  • Prototype Manufacturing: In-house mechanical workshop for turned and milled parts,
    3D Printing (resin and filament printing)

  • Manufacturing network: CNC and laser machining, sheet metal bending parts, welded assemblies, and electronic assemblies through established supplier partners

  • Methodology: DfM/DfA, Requirements Management, Risk Management

Frequently Asked Questions About Collaboration

How does the process of getting started on a project work? We begin with a no-obligation consultation to clarify the project scope, current situation, and goals. Based on this, we prepare a proposal outlining the scope of work and timeline. If you don’t yet have a requirements specification, we’ll help you create one. You can book your first appointment directly online.

Do you handle just entire development projects or also individual tasks? Both. We support projects from the initial idea through design and prototyping all the way to the transition to series production. We also take on specific tasks within existing projects or work long-term as part of our clients’ development teams.

How do we ensure the confidentiality of our development work? Before the project begins, we standardly enter into a non-disclosure agreement that governs our collaboration. We store your project data exclusively on servers we manage ourselves, not in the cloud. For data exchange, we use only services hosted in Europe.

Who owns the results of the development? All rights to the results of the development work belong entirely to our customers. If patents are filed based on a project, our engineers involved are generally named as inventors. Beyond that, we retain no rights whatsoever to the developments.

How are projects billed? For clearly defined work packages, we offer a fixed price. We bill open-ended development phases—whose scope becomes clear only as the project progresses—on a time-and-materials basis. Provided the available information allows it, you will receive a rough estimate of the effort required before work begins. Clients with whom we work regularly often purchase an hourly credit, which we use to flexibly handle various tasks and bill based on time sheets.

Do you work at our office or at your office? We typically work at our office in Munich. There, every project benefits from direct collaboration within the team and the expertise of various colleagues. However, we’re also happy to work at your location for a limited time to help you get up to speed on a project and coordinate with your team.

Do you work with our CAD systems? We use SolidWorks, PTC Creo, Siemens NX, and Autodesk Inventor, which generally allows us to adapt to our customers’ system environments. For data exchange, we use all standard formats, such as STEP, IGES, DXF, and DWG. Upon request, we can also work directly in your PDM system on your servers.

Can you also manufacture prototypes? Yes. In our in-house workshop, we manufacture turned and milled parts as well as 3D-printed parts (resin and filament) for functional models and prototypes. For CNC and laser manufacturing, sheet metal parts, welded assemblies, and electronic assemblies, we rely on a proven network of suppliers.

Do you handle the approval of medical devices? Approval is the responsibility of the manufacturer. We support the process by documenting development decisions, material data, and declarations of conformity (e.g., FDA...), as well as by providing risk management through design FMEA and ensuring that the design is suitable for manufacturing and assembly.

What quality standards does your company follow? Our quality management system is certified to ISO 9001:2015. In the medical technology sector, we have experience with the requirements of ISO 13485 and are working toward obtaining our own certification medium term.

What production volumes do you design for? From small batches of just a few units per year—such as those used in laboratory and research settings—to mass-produced products. Production volume plays a key role in determining manufacturing processes and design, which is why we take it into account from the very beginning.

Our approach to development

We do not regard development as the delivery of results, but rather as taking responsibility for a technically sound solution.

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Our projects demonstrate how this approach has proven effective in practice:

Learn more about our approach and how we work with clients and partners:

Schedule a no-obligation consultation with us:

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