Pulpdent® Activa™ Pronto Universal Stackable Composite Light Cure - FDA Registration CMDR-2025-04534

Access comprehensive regulatory information for Pulpdent® Activa™ Pronto Universal Stackable Composite Light Cure in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04534 and manufactured by Pulpdent Corporation 80 Oakland Street, Watertown, MA 02472, USA Mfd By: Pulpdent Corporation - 300-304 Pleasant Street Watertown, MA 02472, USA in USA. The device was registered on May 06, 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.