Philippines FDA registration CMDR-2025-04177

Pulpdent® Embrace™ Wetbond™ Opaquer Light Cure

Philippines·Pulpdent Corporation - 80 Oakland Street, Watertown, MA 02472, USA·USA·Issued March 20, 2025 – March 20, 2030

Device information

Product Name: Pulpdent® Embrace™ Wetbond™ Opaquer Light Cure
Registration Number: CMDR-2025-04177

Manufacturer details

Manufacturer: Pulpdent Corporation - 80 Oakland Street, Watertown, MA 02472, USA
Country of Origin: USA

Importer & distribution

Importer/Distributor: Surgicom Trading Corp.

Registration dates

Issuance Date: March 20, 2025
Expiry Date: March 20, 2030

About this record

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.