# K103709: Ceracell Dental

- Pathway: 510(k) (Abbreviated)
- Applicant: Curasan AG
- Decided: Mar 10, 2011 after 80 days
- Product code: LYC (Bone Grafting Material, Synthetic)
- Device class: 2
- Regulation: 21 CFR 872.3930
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K941780 (1995). 18 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 20 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K051443: Cerasorb Dental, Cerasorb M Dental and Cerasorb Perio, Curasan Ag, Frankfurt Facility (2005) Summary page 6.

## Most influential descendants
- K111105: Curasan Osseolive Dental (2012), 0 descendants of its own

## Indications for use
Ceracell® DENTAL 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 Filing 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 (GTR) and Guided Bone Regeneration (GBR) Filling of perio-implant defects in conjunction with products intended for Guided Bone Regeneration (GBR)

Source page: https://510kreport.com/device/K103709
Methodology: https://510kreport.com/methodology