# K024139: Aigis-Inlay

- Pathway: 510(k) (Traditional)
- Applicant: Sb Lucius, Inc.
- Decided: Mar 7, 2003 after 81 days
- Product code: EJT (Alloy, Gold-Based Noble Metal)
- Device class: 2
- Regulation: 21 CFR 872.3060
- 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 K951786 (1995). 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)
- K951786: Degulor a, Degussa Corp. (1995) Summary page 1.

## Indications for use
AIGIS-INLAY is intended for manufacturing - Inlay I Onlays - Crowns - Short span bridges - Long span bridges - Removable partials

Source page: https://510kreport.com/device/K024139
Methodology: https://510kreport.com/methodology