Renovis intends to be a leading provider of medical devices and strives to continuously exceed our customers’ expectations of service, quality, reliability, and value.

This is achieved though continuous improvement to commonly-used products in the areas of spine, adult joint reconstruction, and trauma surgery.  Our quality systems were developed to further this goal by ensuring compliance with customer and regulatory requirements.


ISO 13485:2003 Medical devices – Quality management systems – Requirements for regulatory purposes

Renovis Surgical Technologies, Inc. operates a Quality Management System which complies with the requirements of ISO 13485:2003.  The scope of this Quality Management System includes the design, development, manufacture, and distribution of orthopedic and spinal products for orthopedic and spine applications.  Renovis believes its ISO 13485 certification, which is fully recognized in many markets around the world, signifies an unending commitment to the safety and efficacy of the organization’s products.