Helioseal® Light-Curing Fissure Sealant (Refill) - FDA Registration DVR-8466

Access comprehensive regulatory information for Helioseal® Light-Curing Fissure Sealant (Refill) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-8466 and manufactured by Ivoclar Vivadent AG - Bendererstrasse 2, 9494 Schaan, Liechtenstein in Liechtensten. The device was registered on August 11, 2023.

This page provides complete registration details including manufacturer information, importer/distributor details (Alphadent 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.