# K172839: Endosolv

- Pathway: 510(k) (Traditional)
- Applicant: Septodont
- Decided: Feb 13, 2018 after 147 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: 1 generation back to K980633 (1998). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K980633: Endosolv E, Specialites Septodont (1998) Summary page 4.

## Indications for use
Root canal sealers solvent when canal retreatment is required.

Source page: https://510kreport.com/device/K172839
Methodology: https://510kreport.com/methodology