Suture, polypropylene monofilament - ARTG 480706
Access comprehensive regulatory information for Suture, polypropylene monofilament in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 480706 and sponsored by Nobel Biocare Australia Pty Ltd, manufactured by Osteogenics Biomedical Inc in United States of America. The device registration started on February 24, 2025.
This page provides complete registration details including sponsor information, manufacturer details, and regulatory compliance data from the official Australia TGA ARTG medical device database. Pure Global AI offers free access to Australia's complete medical device registry with 131,000+ devices, helping global MedTech companies navigate TGA regulations efficiently.
The creos™ syntostitch PTFE Suture is intended for use in soft tissue approximation and ligation in the oral cavity and is suitable for various dental surgical procedures. This device is designed for short-term use and requires removal after the healing phase. It is not indicated for cardiovascular, ophthalmic, microsurgical, or central/peripheral neural tissue procedures. This suture provides effective support for the healing of soft tissues in dental surgeries, contributing to improved procedural outcomes in oral surgical interventions.