# K050260: Bioresorb Macro Pore

- Pathway: 510(k) (Traditional)
- Applicant: Oraltronics Dental Implant Technology GmbH
- Decided: Jul 15, 2005 after 162 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: 1 generation back to K014156 (2002). 1 ancestor in all.
4 later devices descend from it; 2 cite it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K014156: Cerasorb Ortho, Curasan AG (2002)

## Most influential descendants
- K083372: Arrowbone-a, Arrowbone-B (2009), 1 descendant of its own
- K081561: Osferion D (2008), 1 descendant of its own
- K110198: Blue Sky Bio TCP (2011), 0 descendants of its own
- K091618: Vitomatrix (2010), 0 descendants of its own

## Indications for use
BioResorb® is to be used as a bone void filler device used in guided tissue regeneration, sinus lifts, ridge maintenance, alveolar socket preservation or ridge augmentation, and the treatment of osseous defects.

Source page: https://510kreport.com/device/K050260
Methodology: https://510kreport.com/methodology