Ximedica Product Development | Creating devices that deliver safe, repeatable outcomes

Through all phases of medical device development, our expert designers, engineers, and project managers collaborate with your team to align your medical device development efforts with FDA expectations and gain faster regulatory approvals.

Our proven, integrated medical device development process, with an emphasis on human factors engineering, allows us to create ISO 13485 medical devices that are thoughtfully designed, approved, manufactured and ultimately delivered to market.

Our Proven Process  

Research, Strategy, & Concept Generation
Concept & Requirements Development
Detailed Design Development
Design Verification
Process Validation, Manufacturing Transfer, & Design Validation
Production & Commercial Support

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