Pulpdent® Embrace™ Wetbond™ Opaquer Light Cure - FDA Registration CMDR-2025-04177

Access comprehensive regulatory information for Pulpdent® Embrace™ Wetbond™ Opaquer Light Cure in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04177 and manufactured by Pulpdent Corporation - 80 Oakland Street, Watertown, MA 02472, USA in USA. The device was registered on March 20, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Surgicom Trading Corp.), 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.