


Getting your medical device from idea to production can feel overwhelming. Once you know what you want to do, next steps can be a little confusing, and missing a step can result in missed deadlines and other problems that delay your launch and cause additional stress.
You deserve to end up with an end product that meets or exceeds your expectations — one that’s a true success. That’s why it’s critical to work with a team you trust, one who understands your vision and will help you keep your project on track.

Well-designed medical devices can be life-changing for both user and designer. At C3 Medical Device Consulting, we’ve helped everyone from startups to large corporations successfully design medical devices and get FDA approval, many of which are now thriving on the market.
By the end of our design audit, you’ll be able to successfully answer the following questions:
Ensure your device is built to last as our team walks you through protocol assessment requirements.
Verify your device meets FDA guidelines, passes risk analysis, and excludes failure potentials.
Confirm your device will be production-ready and meets all manufacturer requirements.
We’ve helped hundreds of customers across the nation turn their medical device designs into usable products that successfully make it to market — now, we’re ready to do the same for you.
“C3 went above and beyond, and set the bar for me in terms of how I define an invested 3rd party. C3 felt more like an internal team who was there to see the product be successful above all else. If they want to work with you, it’s because they care about your product and are excited to see it succeed. ”
Avatech, Inc. Chief Product Officer
Turning your idea for a medical device into a tangible, market-ready product can be overwhelming. A free medical device audit from our team of experienced medical device consultants will tell you what’s missing on your device, suggest helpful design improvements, and provide a clear plan moving forward, bringing you one step closer to getting your medical device to market.
Sign up for a free design audit.
Our team will reach out within 24 hours to gather more information on your device.
Receive a clear plan forward so your device exceeds all expectations and thrives on the market.








Take the guesswork out of the equation with our budgeting calculator and empower yourself to focus on what really matters:
Bringing innovation to life.

At C3 Medical Device Consulting, we understand that transforming a concept into a market-ready medical device can be a complex journey. Our team of seasoned consultants is dedicated to guiding you through each step, ensuring that your device not only meets regulatory standards but also aligns with market needs and user expectations.
With our extensive experience in the medical device industry, we have the knowledge and resources to help you navigate the intricacies of design and compliance. From initial concept validation to final FDA approval, we provide tailored support that empowers you to achieve your goals efficiently and effectively.
Choosing the right consulting partner is crucial for the success of your medical device project. C3 Medical stands out due to our commitment to excellence, personalized service, and a proven track record of helping clients realize their vision. Our free design audit is just the first step in a collaborative process aimed at optimizing your device.
Our team not only identifies potential compliance issues but also offers actionable insights and recommendations to enhance your design. By leveraging our expertise, you can significantly reduce the time and cost associated with bringing your medical device to market, making us the ideal choice for your consulting needs.
Regulatory compliance is a fundamental aspect of medical device development that cannot be overlooked. Ensuring that your device meets the required standards is essential not only for gaining FDA approval but also for ensuring patient safety and market success. Our design audit addresses these critical compliance factors comprehensively.
We help you understand the regulatory landscape, guiding you through the necessary documentation and testing protocols. By prioritizing compliance from the outset, you can mitigate risks and avoid costly delays, ultimately leading to a smoother path to market entry.
Success stories from our clients showcase the effectiveness of our consulting services. We have helped numerous startups and established companies alike turn their innovative medical device concepts into successful products. Our hands-on approach and tailored solutions have been instrumental in overcoming challenges and achieving market readiness.
For example, one of our clients, a startup in the orthopedic sector, leveraged our design audit to refine their product concept and navigate the regulatory process. As a result, they successfully launched their device within a year, receiving positive feedback from both healthcare professionals and patients. These stories reflect our dedication to client success and the tangible results of our partnership.