Quality Standards

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. In addition, Springboard is ISO 9001 certified.

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.

Phone: 916-853-0717
Fax: 916-853-0711
Email: help@springboardmfg.com

2691 Mercantile Drive, Rancho Cordova, CA 95742
404 West 8th Street, Kearney, NE 68845
3525 Haven Ave, Menlo Park, CA 94025



Plastic Injection Molding

In-Process QC and Product Testing

Multi-Component Product Assembly

Special Packaging




Contact Us