3M Espe Vitrebond Light Cure Glass Ionomer Linear/Base - FDA Registration DVR-3600

Access comprehensive regulatory information for 3M Espe Vitrebond Light Cure Glass Ionomer Linear/Base in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-3600 and manufactured by 3M Espe Dental Products 2510 Conway Avenue, St. Paul, Minnesota, 55144-1000 U.S.A in USA. The device was registered on March 21, 2023.

This page provides complete registration details including manufacturer information, importer/distributor details (3M Philippines, Inc.), 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.