Ferry Machine Corp - Manufacturing Precision Tools and Components

Established in 1952, Ferry Machine began as a manufacturer of precision military and aircraft components that supplied the U.S. Department of Defense. In the mid-1980s, the New Jersey-based company moved into new markets such as optical components, as well as precision instruments and other products for the medical industry. Ferry Machine takes pride in its responsiveness to client needs and delivers on-time performance and expedited turnaround as required. The company earned Stryker Orthopaedics recognition as Specialty Instruments Supplier of the Year in 2008 and 2011.

At the core of Ferry Machine’s offerings are CNC machining services that fulfill a wide range of precision engineering needs, from end-consumer products to machine tools and parts. The company’s state-of-the-art equipment ensures unparalleled accuracy, even with extremely complex designs. CAD/CAM machine-turning equipment ensures that all products are precisely tested while safeguarding their integrity. To learn more about the company’s CNC milling and turning capacities, visit www.ferrymachine.com.

A Brief Explanation of ISO 13485 Certification

Orthopedic instrumentation and implants manufacturer Ferry Machine has operated from its headquarters in Little Ferry, New Jersey, since its founding in 1952. As a testament to its commitment to excellence, Ferry Machine has attained International Organization for Standardization (ISO) certifications 9001: 2008 and 13845: 2003 for its regular and medical quality management systems, respectively. The ISO 13485: 2003 certification specifically applies to organizations that need to demonstrate capabilities to provide medical devices.

Because the ISO 13845 standard focuses on medical devices, it includes some particular requirements for medical devices, while excluding some ISO 9001 requirements. However, organizations may find benefit in achieving both ISO 9001 and 13845 standards, since 9001 focuses on high-value business practices. ISO 13485 focuses on meeting regulatory and customer requirements while maintaining effective processes and risk management.

In addition, 13485 helps organizations create a management system that provides a framework for compliance with the Federal Drug Administration and other regulatory mandates. Organizations seeking to achieve ISO 13485 certification should first understand regulatory and customer requirements, along with gaining knowledge of what a 13485-compliant management system entails.