# K202413: LC ResinCal PC

- Pathway: 510(k) (Traditional)
- Applicant: S&C Polymer Silicon- Und Composite Spezialitaten GmbH
- Decided: Nov 20, 2020 after 88 days
- Product code: EJK (Liner, Cavity, Calcium Hydroxide)
- Device class: 2
- Regulation: 21 CFR 872.3250
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K922721 (1992). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K063237: Theracal LC, Bisco, Inc. (2006) Summary page 4.

## Indications for use
1. Pulp capping agent 2. Liner

Source page: https://510kreport.com/device/K202413
Methodology: https://510kreport.com/methodology