# K875133: Cavit-W

- Pathway: 510(k) (Traditional)
- Applicant: Espe GmbH (Us)
- Decided: Mar 1, 1988 after 77 days
- Product code: EBG (Crown And Bridge, Temporary, Resin)
- Device class: 2
- Regulation: 21 CFR 872.3770
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
11 later devices descend from it; 3 cite it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K092715: Iroot BP Plus (2009), 7 descendants of its own
- K102867: Iroot FS (2010), 2 descendants of its own
- K240365: Bioceramic Root Repair Material (C-Root BP) (2024), 1 descendant of its own
- K061530: MD-Temp (2006), 1 descendant of its own
- K251465: Root canal repair materials (nRoot BP) (2025), 0 descendants of its own

Source page: https://510kreport.com/device/K875133
Methodology: https://510kreport.com/methodology