IMEQ offers a comprehensive Design & Engineering Service that bridges the gap between concept and market-ready medical devices. With a robust portfolio of existing products—including implants, instruments, and surgical tools—IMEQs leverages its in-house expertise to customize these offerings or develop entirely new solutions tailored to specific clinical needs. This capability enables IMEQs to support clients at any stage of the product lifecycle, from initial design through to regulatory approval and manufacturing.
The service integrates advanced engineering techniques such as 3D modeling, finite element analysis (FEA), and rapid prototyping to ensure designs are both innovative and manufacturable. IMEQs' team collaborates closely with clients to understand their unique requirements, providing solutions that are compliant with global standards like ISO 13485, MDR, and FDA regulations. Whether adapting an existing product or creating a new one, IMEQs' Design & Engineering Service delivers high-quality, reliable medical devices that meet the evolving needs of the healthcare industry.
Precision Meets Expertise
IMEQ combines deep industry knowledge with hands-on engineering expertise to deliver tailored medical device solutions that truly work. With a proven track record in osteosynthesis and related fields, we understand both clinical needs and manufacturing realities. Partnering with IMEQs means you gain a collaborative team focused on innovation, regulatory compliance, and practical design—helping you bring safe, effective products to market faster and with greater confidence.
Tailored Solutions
We customize each design to fit your specific clinical requirements and manufacturing capabilities, ensuring the final product meets both functional and practical needs.
Advanced Engineering
Utilizing cutting-edge 3D CAD modeling, finite element analysis (FEA), and rapid prototyping, we create precise and thoroughly tested designs that perform reliably in real-world applications.
Regulatory Focus
Our design process integrates key global compliance standards such as ISO 13485, MDR, and FDA regulations, helping streamline regulatory approval and market entry.
Collaborative Process
IMEQ works closely with your team throughout development, maintaining open communication to align design decisions with your business objectives and project timelines.
Vision Meets Precision
At IMEQ, our design process is structured to deliver precision, efficiency, and compliance at every stage. Leveraging our extensive experience with our own line of trusted implants and instruments, we collaborate closely with clients—combining technical expertise and industry best practices—to ensure your product moves smoothly from concept to production.
- Consultation
- Concept Development
- 3D Design
- Simulation
- Prototyping
- Finalization
Frequently asked questions
Yes, we specialize in adapting and optimizing our existing implant designs to fit your specific clinical requirements and manufacturing processes.
Absolutely. We collaborate from the very beginning, turning initial ideas into detailed, viable designs ready for prototyping and production.
We use rapid prototyping techniques to produce physical models quickly, allowing you to evaluate and refine the design early in the development process.
Yes, all designs are developed following global regulatory standards such as ISO 13485, MDR, and FDA requirements to facilitate smooth market approval.
We prepare complete and detailed technical files and design history documentation to support regulatory submissions and audits.