PULPDENT® EMBRACE™ WETBOND™ SEAL-N-SHINE™ Light Cure Resin - FDA Registration CMDR-2024-02869

Access comprehensive regulatory information for PULPDENT® EMBRACE™ WETBOND™ SEAL-N-SHINE™ Light Cure Resin in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2024-02869 and manufactured by Pulpdent Corporation 80 Oakland Street, Watertown, MA 02472 USA in USA. The device was registered on May 16, 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.