# K171050: Geistlich Fibro-Gide

- Pathway: 510(k) (Traditional)
- Applicant: Geistlich Pharma AG
- Decided: Nov 9, 2017 after 216 days
- Product code: NPL (Barrier, Animal Source, Intraoral)
- 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: 7 generations back to K924408 (1995). 11 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K102531: Mucograft, Ed. Geistlich Soehne AG Fur Chemische Industrie (2010) Summary page 4.

## Most influential descendants
- K252253: Geistlich Mucograft® /Geistlich Mucograft®  Seal; Geistlich Fibro-Gide® (2025), 0 descendants of its own

## Indications for use
Geistlich Fibro-Gide® is intended for soft tissue augmentation. It is indicated for: Localized gingival augmentation to increase keratinized tissue (KT) around teeth and implants Alveolar ridge reconstruction for prosthetic treatment Recession defects for root coverage

Source page: https://510kreport.com/device/K171050
Methodology: https://510kreport.com/methodology