Precision manufacturing with state-of-the-art processes
Our processes capabilities
We take pride in our rigorous processes that ensure the highest quality standards for our medical device OEM partners. Our ISO 13485 certification and FDA registration reflect our commitment to quality and regulatory compliance.
State-of-the-art inspection capabilities
Our inspection capabilities are designed to meet the most demanding requirements of the medical device industry. Our CMM machines provide precise and reliable measurements of complex geometries. Our Vision Systems perform automated inspection of critical features and detect defects with high accuracy. Our FAI process ensures that every part we produce meets the specifications and requirements of our customers.
Clean room assembly and packaging
Our clean room assembly and packaging capabilities provide a controlled environment for the production of sterile medical devices. We strictly adhere to industry standards and regulations to ensure the safety and efficiency of the devices we produce. Our clean room facilities are equipped with the latest technology to minimize contamination risks and ensure the highest quality standards.
We understand the importance of regulatory compliance in the medical device industry. Our ISO 13485 certification and FDA registration demonstrate our commitment to meeting the highest standards for quality and safety. We work closely with our customers to ensure that their products meet all regulatory requirements and that all necessary documentation is provided to support their regulatory filings.