About
IMDS Consulting specializes in guiding medical device manufacturers through the complexities of FDA compliance and regulatory submissions. Led by President Isaac Erickson, a seasoned expert with over 15 years of experience, we provide strategic regulatory support tailored to achieve 510(k) clearances, Class I and Class II submissions, Class III PMAs, and international product registrations. Our mission is to bridge the gap between innovative product development and stringent regulatory standards, ensuring that your medical devices achieve market success while maintaining full compliance. About Us: IMDS Consulting offers a full suite of regulatory and product development services, including: FDA Submissions: Expertise in 510(k) clearances, eSTAR applications, Class III PMAs, and UDI implementation. International Registrations: Guidance for entering markets in Mexico, Peru, Colombia, EU and beyond. Let IMDS Consulting simplify your regulatory journey and elevate your innovation
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Company Information
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Employees 1
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Founded 2024
