# K023976: Acroseal Root Canal or Apical Sealer

- Pathway: 510(k) (Traditional)
- Applicant: Septodont S.A.S.
- Decided: Jan 30, 2003 after 64 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
Permanent canal filling

Source page: https://510kreport.com/device/K023976
Methodology: https://510kreport.com/methodology