We have over 20 years experience in helping companies and institutions move their medical device through the FDA.
RFD's, Q-Subs, Class I, II and III; 510(k), De Novo, PMA's. Post-marketing surveillance and compliance.
Fox started their work with 3D Printing way back in 1988! The technology has come a long way. Today, Fox leverages their industry-acknowledged leadership to manufacture FDA approved parts and devices through 3D Printing.
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Fox has developed TekniGROW™ - a trademarked and effective product development process certification. TekniGROW™ takes a comprehensive and disciplined approach to both evaluate and develop technology breakthroughs.