RegenerOss Resorbable Xenograft - India CDSCO Medical Device Registration

RegenerOss Resorbable Xenograft is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000266_5374378274d6b16fd63f89443e4c1962_1e72c5bbdd50fb8ba5f629a2c2b2c2df. 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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CDSCO Registered

Class Class D

RegenerOss Resorbable Xenograft

UID: IMP/MD/2021/000266_5374378274d6b16fd63f89443e4c1962_1e72c5bbdd50fb8ba5f629a2c2b2c2df

Brand Name

RegenerOss Resorbable Xenograft Syringe

License Holder

ZB Dental India Pvt Ltd

Device Class

Class D

Approving Authority

CDSCO

Product Information

RegenerOss® Resorbable Xenograft is indicated 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).