# K072069: Spacer

- Pathway: 510(k) (Traditional)
- Applicant: Vericom Co., Ltd.
- Decided: Sep 28, 2007 after 60 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: 1 generation back to K926418 (1993). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K926418: CLIP, Voco GmbH (1993) Summary page 1.

## Indications for use
Temporary restoration of inlay and onlay preparations Temporary fillings and sealings

Source page: https://510kreport.com/device/K072069
Methodology: https://510kreport.com/methodology