PULPDENT FORENDO Paste Calcium Hydroxide with Iodoform Root Canal Treatment Paste - FDA Registration CMDR-2024-02323

Access comprehensive regulatory information for PULPDENT FORENDO Paste Calcium Hydroxide with Iodoform Root Canal Treatment Paste in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2024-02323 and manufactured by Pulpdent Corporation 80 Oakland Street, Watertown, MA 02472, USA in USA. The device was registered on January 30, 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.