# K262050: Vioseal X

- Pathway: 510(k) (Traditional)
- Applicant: Spident Co., Ltd.
- Decided: Sep 11, 2026 after 85 days
- Product code: KIF (Resin, Root Canal Filling)
- Device class: 2
- Regulation: 21 CFR 872.3820
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 8 generations back to K990131 (1999). 30 ancestors in all.
No later device cites it as a predicate yet.
0 of 31 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K190503: CeraSeal, Meta Biomed Co., Ltd. (2019) Summary page 5.

## Indications for use
Permanent obturation of the root canal following vital pulp extirpation

Source page: https://510kreport.com/device/K262050
Methodology: https://510kreport.com/methodology