PERMAFLO® FLOWABLE COMPOSITE - FDA Registration MDR-0741

Access comprehensive regulatory information for PERMAFLO® FLOWABLE COMPOSITE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-0741 and manufactured by Ultradent Products, Inc. - 505 West Ultradent Drive (10200 South ) South Jordan, Utah 84095 USA in USA. The device was registered on August 06, 2024.

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