From Prototype Design to Full Production Capabilities

Zhifan understands deeply that successful products and customer relationships are the result of manufacturability design creativity, the ability to provide strict tolerances, and the expertise gained from insights through iterative processes. Our engineers work with your design team to manufacture medical device parts, and our knowledge and experience with FDA regulatory requirements add direct value to our relationships.
In the prototype design phase, we first produce several sample parts to assist your design engineers with concept validation. Then, we assist in iterations during the prototype design phase, quickly responding to design changes. We can complete necessary dynamic changes to bring your new product to market faster. We work directly with your design engineers to evaluate manufacturability and material choices to avoid potential quality issues. Therefore, when your precision medical device design is ready for clinical trials and FDA or other regulatory approvals, we begin building strong processes and documentation that will play a crucial role in your product's future success. At last, we focus on continuous improvement of internal management processes to reduce costs and delivery time, which has a positive impact on the quality of the parts we provide you. Once market recognition is achieved, we handle high-precision, tight-tolerance, and large-volume parts machining to meet your monthly and annual needs.