Quality Standards & Certifications


ISO 13485 Certified for Medical Component Manufacturing

Springboard is ISO 13485 certified. “ISO 13485: Medical Devices—Quality Management Systems—Requirements for Regulatory Purposes” is an ISO standard that states the requirements for a comprehensive quality management system for the design/manufacture of medical components and sub-assemblies.

As stated on ISO.org, the ISO 13485 standard “specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical [components] and related services that consistently meet custom and applicable regulatory requirements. Such organizations can be involved in […] design and development, production, storage and distribution, installation, or servicing of a medical [component] and development or provision of [technical support]” or any combination of these processes.

Quality Standards for Your Unique Requirements

As needed, Springboard will work with you to develop a customized set of standards for your individual project. We can meet the quality demands of nearly any industry or application. Contact us to discuss your unique quality requirements. 

Springboard: Quality You Can Depend On

No matter what your industry or application, the quality of your injection molded parts and products is our #1 priority. Request a quote today to get your project started, or contact Springboard to learn more about our quality standards and certifications.

Not sure what plastic you need for your next project? Contact us today!