# K210280: Geistlich Mucograft®, Geistlich Mucograft® Seal

- Pathway: 510(k) (Special)
- Applicant: Geistlich Pharma AG
- Decided: Mar 3, 2021 after 30 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: 9 generations back to K924408 (1995). 26 ancestors in all.
3 later devices descend from it; 3 cite it directly.
0 of 30 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K192042: Geistlich Bio-Gide, Geistlich Bio-Gide Shape, Geistlich Bio-Gide Compressed, Geistlich Bio-Gide Perio, Geistlich Combi-Kit Collagen, Geistlich Perio-System Combi-Pack, Geistlich Mucograft and Geistlich Mucograft Seal, Geistlich Pharma AG (2019) Summary page 4.
- K140518: Geistlich Mucograft: 15 X 20 MM, 20 X 30 MM, 8 MM Diameter, Geistlich Pharma AG (2014) Summary page 4.
- K102531: Mucograft, Ed. Geistlich Soehne AG Fur Chemische Industrie (2010) Summary page 4.
- K073711: Mucograft Collagen Matrix, Ed. Geistlich Soehne AG Fuer Chemische Industrie (2008) Summary page 4.

## Most influential descendants
- K250512: Augmented Gingival Matrix (2025), 0 descendants of its own
- K252253: Geistlich Mucograft® /Geistlich Mucograft®  Seal; Geistlich Fibro-Gide® (2025), 0 descendants of its own
- K233203: Soft Tissue Augmentation Resorbable Matrix (2024), 0 descendants of its own

## Indications for use
Geistlich Mucograft® and Geistlich Mucograft® Seal are indicated for: • covering of implants placed in immediate or delayed extraction sockets; • localized gingival augmentation to increase keratinized tissue (KT) around teeth and implants; • alveolar ridge reconstruction for prosthetic treatment; and • recession defects for root coverage.

Source page: https://510kreport.com/device/K210280
Methodology: https://510kreport.com/methodology