3M FILTEK™ P6 POSTERIOR RESTORATIVE - FDA Registration DVR-3585

Access comprehensive regulatory information for 3M FILTEK™ P6 POSTERIOR RESTORATIVE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-3585 and manufactured by 3M, Espe Dental Products - 2510 Conway Avenue St. Paul MN 55144, USA in USA. The device was registered on August 02, 2024.

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.