Philippines FDA registration MDR-00488

Filtek™ Z250 XT NANO HYBRID UNIVERSAL RESTORATIVE

Philippines flagPhilippines·3m Espe Dental Products - 2510 Conway Avenue St. Paul MN 55144, USA·USA·Issued July 09, 2025 – March 28, 2029
Device information
Product Name
Filtek™ Z250 XT NANO HYBRID UNIVERSAL RESTORATIVE
Registration Number
MDR-00488
Manufacturer details
Country of Origin
USA
Importer & distribution
Importer/Distributor
Alphadent Corporation
Registration dates
Issuance Date
July 09, 2025
Expiry Date
March 28, 2029
About this record

Access comprehensive regulatory information for Filtek™ Z250 XT NANO HYBRID UNIVERSAL RESTORATIVE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-00488 and manufactured by 3m Espe Dental Products - 2510 Conway Avenue St. Paul MN 55144, USA in USA. The device was registered on July 09, 2025.

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.

Free DatabasePowered by Pure Global AIFDA Official DataUSA