With years of expertise, we specialize in rapid, straightforward medical device engineering solutions. Our services encompass the entire development process, from initial concept to production and post-market surveillance.
With a focus on innovation we consistently surpass expectations. We work closely with Quality Management and Regulatory Affairs to ensure seamless compliance and exceptional outcomes.
Our commitment to quality is unlimited. We are proud to be ISO 13485 certified, demonstrating our adherence to rigorous standards.
Lizard provides flexible product development services from concept to completion, including feasibility studies, design concepts, and testing. Our capabilities include prototype production, testing facilitation, and transitioning designs to manufacturing sites.
We assist in obtaining FDA and CE certifications and offer post-market surveillance. Clients can customize engineering and manufacturing services to their needs for tailored solutions.
Initially, we focus on defining product specifications, performing market research, and, if applicable, initiating a patent application. A feasibility study may also be conducted to assess the viability of the project.
In this phase, we develop the design using various methods to provide a wide range of solutions to meet our clients' needs. With our years of experience, we design every stage, offering full support to our clients. We assist our customers in obtaining rapid market access and product approvals, including those for Europe and the US. Furthermore, we coordinate biomechanical and chemical testing to meet all necessary criteria.
To deliver functional, intelligent, and intuitive solutions, we employ finite element methods to enhance our designs. Moreover, we optimize the topology of components and products to simplify manufacturing, reduce weight, and save time and costs.
Whether during the conception or design phase, we offer initial parts to clients for visual and functional assessment, through Voice of Customer feedback or Cadaver Lab testing. With our diverse materials and in-house 3D printing technologies, coupled with our extensive network, we're committed to delivering prompt and proactive support, staying one step ahead.
Alignment with our quality system is crucial throughout the development process. Our dedicated quality and regulatory team is involved at every stage, offering full support to our clients. We assist our customers in obtaining rapid market access and product approvals, including those for Europe and the US. Furthermore, we coordinate biomechanical and chemical testing to meet all necessary criteria.
With our broad network, we convert designs (2D, 3D) into actual products and set up the manufacturing and post-processing flow. As an accredited contract manufacturer, we manage organization, quotations, inspections, and documentation. Our goal is to fully support our customers throughout these stages.
The final stage in the product cycle involves conducting post-market surveillance. This allows us to understand the end-user needs better. This valuable insight and experience drive the enhancement of our products and spark innovative ideas. Additionally, we collaborate closely with surgeons, providing training on specialized instrumentation devices.
If you are interested in collaborating with us, please get in touch
