# K153127: everX Posterior

- Pathway: 510(k) (Traditional)
- Applicant: GC America, Inc.
- Decided: May 20, 2016 after 204 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: 3 generations back to K041474 (2004). 4 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K102703: Build-IT Total Core, Pentron Clinical (2011) Summary page 4.

## Most influential descendants
- K192260: everX Flow (2019), 0 descendants of its own

## Indications for use
everX Posterior is indicated for use as a fiber reinforced composite for the restoration of prepared carious teeth, including large posterior cavities with loss of dentin.

Source page: https://510kreport.com/device/K153127
Methodology: https://510kreport.com/methodology