MEDPOR Customized Cranial Implant - Prosthesis, internal, ear/nose/throat, synthetic
Access comprehensive regulatory information for MEDPOR Customized Cranial Implant - Prosthesis, internal, ear/nose/throat, synthetic in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is sponsored by Stryker Australia Pty Ltd, manufactured by Stryker Leibinger GmbH & Co KG in Germany. The device registration started on January 17, 2024.
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 MEDPOR Customized Implant is indicated for the augmentation and/or restoration of bony and/or soft tissue deformities in post-traumatic, post-surgical, or congenital craniofacial defects, including, but not limited to, the correction and prevention of persistent temporal hollowing (PTH), in the adult population.