Pulpdent® Liquid Cavity Liner - FDA Registration CMDR-2024-03245

Access comprehensive regulatory information for Pulpdent® Liquid Cavity Liner in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2024-03245 and manufactured by Pulpdent Corporation - 80 Oakland Street, Watertown, MA 02472, USA in USA. The device was registered on September 18, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (Surgicom Trading Corporation), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.