# K251390: MTA vpt

- Pathway: 510(k) (Traditional)
- Applicant: Voco GmbH
- Decided: Jul 3, 2025 after 59 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
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
- Indirect pulp capping - Direct pulp capping - Pulpotomy, after removal of affected coronal pulp to preserve vitality of remaining pulp tissue

Source page: https://510kreport.com/device/K251390
Methodology: https://510kreport.com/methodology