Pulpdent® Lime-Lite™ Enhanced Light Cure Cavity Liner

Access comprehensive regulatory information for Pulpdent® Lime-Lite™ Enhanced Light Cure Cavity Liner in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2024-02404 and manufactured by Pulpdent Corporation 80 Oakland Street, Watertown, MA 02472, USA in USA. The device was registered on March 04, 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.