Synthetic Mineral-Collagen Composite Bone Graft
- UID
- IMP/MD/2021/000266_e0fea3a14f42989cdfb06104346dd381_9147002cbf4db716a77f4ddb3df87bd6
- Device class
- Class D
- Brand name
- RegenerOss Resorbable Xenograft Syringe
- License holder
- ZB Dental India Pvt Ltd
- Approving authority
- CDSCO
- Product information
- RegenerOss Synthetic is recommended for: - Augmentation or reconstructive treatment of the alveolar ridge. - Filling of infrabony periodontal defects. - Filling of defects after root resection, apicoectomy, and cystectomy. - Filling of extraction sockets to enhance preservation of the alveolar ridge. - Elevation of the maxillary sinus floor. - Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (RegenerOss Resorbable Xenograft Syringe) and Guided Bone Regeneration (RegenerOss Resorbable Xenograft Syringe). - Filling of peri-implant defects in conjunction with products intended for Guided Bone Regeneration (RegenerOss Resorbable Xenograft Syringe)
Synthetic Mineral-Collagen Composite Bone Graft is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000266_e0fea3a14f42989cdfb06104346dd381_9147002cbf4db716a77f4ddb3df87bd6. This device is marketed under the brand name RegenerOss Resorbable Xenograft Syringe. The license holder is ZB Dental India Pvt Ltd, and it is classified as Device Class Class D. The approving authority is CDSCO.
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