Verify our credentials on the National eGov Portal.
FlexiOss® is a registered medical device with the Philippines Food and Drug Administration. We publish our registration numbers openly so any surgeon, hospital procurement officer or patient can confirm our standing against the official government record — no intermediaries.
Certificates of Medical Device Registration
FlexiOss® Ortho
CMDR-2025-04943A
Orthopedic & trauma bone reconstruction
FlexiOss® Dent
CMDR-2025-04943B
Dental, dentoalveolar & maxillofacial grafting
What the government record confirms
The active Certificate of Medical Device Registration (CMDR) number issued for each FlexiOss® product line.
The registered importer and exclusive nationwide distributor of record, Fortschritt Medical Supplies Inc.
The device classification and intended use approved for the Philippine market under prevailing FDA Circulars.
The current registration status and validity window, maintained directly within the national regulatory system.
Check our compliance at the source.
The eGov PH platform consolidates Philippine government services, including regulatory and FDA-related verifications, under one official portal. Registration of imported medical devices and the conduct of their distributors are governed by prevailing FDA Circulars; the eGov system is the public entry point for confirming that standing in real time.
Registration numbers and statuses are maintained by the Philippines Food and Drug Administration and may be updated through new Circulars or directives. Always confirm the current record directly on the official government portal.