Medical Device Post-Production Services, Inc.

Medical Device Post-Production Services, Inc. (MDPPS) is a regulatory and compliance consulting firm specializing in enabling foreign medical device manufacturers to commercialize products in the United States. Core services include acting as a U.S. Agent for device registration and sales, Initial Importer representation for FDA compliance, and strategic consulting on Quality Management Systems (QMS), device design and development, manufacturing strategy, and regulatory/standards compliance. MDPPS guides clients through FDA establishment registration, medical device reporting requirements, and the full import/regulatory pathway to market entry. The firm serves as a bridge between international device manufacturers and U.S. regulatory frameworks, handling documentation, customs coordination, and compliance validation to streamline device commercialization.