# K102872: Osbone Dental

- Pathway: 510(k) (Traditional)
- Applicant: Curasan AG
- Decided: Jan 12, 2011 after 104 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: 2 generations back to K852742 (1985). 7 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K873763: Bio-Oss - Ceramic Pure Natural Hydroxyapatite, Geistlich-Pharma (1987) Summary page 1.
- K980679: Endobon, Biomet, Inc. (1998) Summary page 1.
- K072056: Osteograf/D-700, Dentsply International, Inc. (2007) Summary page 1.

## Most influential descendants
- K202675: InRoad® Dental Synthetic Bone Graft (2022), 0 descendants of its own

## Indications for use
Osbone® DENTAL is intended for the filling and reconstruction of multi-walled bone defects, e.g.: Defects after removal of bone cysts Augmentation of the atrophied alveolar ridge Sinus lift and sinus floor elevation (subantral augmentation) Filling of alveolar defects following tooth extraction for alveolar ridge preservation Filling of extraction defects to create an implant bed Filling of two- or multi-walled infrabony pockets, and bi- and trifurcation defects Support function for a membrane in controlled tissue regeneration (CTR) Defects after surgical removal of retained teeth or corrective osteotomies Other multi-walled bone defects of the alveolar processes.

Source page: https://510kreport.com/device/K102872
Methodology: https://510kreport.com/methodology