# K980633: Endosolv E

- Pathway: 510(k) (Traditional)
- Applicant: Specialites Septodont
- Decided: May 1, 1998 after 71 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.
1 later device descends from it; 1 cites it directly.
0 of 2 devices 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.

## Most influential descendants
- K172839: Endosolv (2018), 0 descendants of its own

## Indications for use
Softening and removal of root canal fillings

Source page: https://510kreport.com/device/K980633
Methodology: https://510kreport.com/methodology