Philippines FDA registration DVR-3585

3M FILTEK™ P6 POSTERIOR RESTORATIVE

Philippines·3M, Espe Dental Products - 2510 Conway Avenue St. Paul MN 55144, USA·USA·Issued August 02, 2024 – January 22, 2029

Device information

Product Name: 3M FILTEK™ P6 POSTERIOR RESTORATIVE
Registration Number: DVR-3585

Manufacturer details

Manufacturer: 3M, Espe Dental Products - 2510 Conway Avenue St. Paul MN 55144, USA
Country of Origin: USA

Importer & distribution

Importer/Distributor: Alphadent Corporation

Registration dates

Issuance Date: August 02, 2024
Expiry Date: January 22, 2029

About this record

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.