# K990982: Cavit LC

- Pathway: 510(k) (Traditional)
- Applicant: Espe Dental AG
- Decided: Apr 23, 1999 after 30 days
- Product code: EBF (Material, Tooth Shade, Resin)
- Device class: 2
- Regulation: 21 CFR 872.3690
- 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 K926418 (1993). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K972892: Cavit-LC, Espe GmbH & Co. Kg. (1997) Summary page 1.

## Indications for use
Temporary fillings Temporary management of inlay and onlay preparations Temporary closure of implant screw holes Relining of temporary pre-made crowns and bridges

Source page: https://510kreport.com/device/K990982
Methodology: https://510kreport.com/methodology