FDA Registered and ISO 13485 Certified, Ximedica provides the right talent and expertise to get you to market with the right product at the right time. With 30 years of experience and hundreds of satisfied clients in healthcare, Ximedica can launch FDA compliant devices faster and with higher market adoption.
Ximedica’s quality assurance measures ensure that your medical device is safe for the end-user in addition to being commercially viable. With facilities in San Francisco, Minneapolis, Providence, and Hong Kong, our expert team of designers, engineers, and project managers use a human-centered, integrated development process to create innovative medical devices that are thoughtfully designed, approved, manufactured and ultimately delivered to market.
