Australia TGA ARTG recordNeomem FLEXPLUS - Collagen dental regeneration membrane
Australia TGA ARTG Registered Device · My Biologics Pty Ltd · Collagen Matrix Inc · Class III · Started May 28, 2019
Good Name: My Biologics Pty Ltd - Neomem FLEXPLUS - Collagen dental regeneration membrane
- Risk Class
- Class III
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- May 28, 2019
- Effective Date
- May 28, 2019
- Country
- United States of America
- Address
- 15 Thornton Road, Oakland, NJ, 07436
This resorbable porcine collagen dental membrane is a bioresorbable, implantable collagen material that is intended for use in oral surgical procedures as a resorbable membrane material for use in, simultaneous use of guided bone regeneration (GBR)-membrane and implants; augmentation around implants placed in immediate extraction sockets; augmentation around implants placed in delayed extraction sockets; localized ridge augmentation for later implantation; alveolar ridge reconstruction for prosthetic treatment; filling of bone defects after root resection, cystectomy or removal of retained teeth; guided bone regeneration in dehiscence defects; guided tissue regeneration in periodontal defects.
Access comprehensive regulatory information for Neomem FLEXPLUS - Collagen dental regeneration membrane in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is sponsored by My Biologics Pty Ltd, manufactured by Collagen Matrix Inc in United States of America. The device registration started on May 28, 2019.
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.