# K993475: Aurofluid M, Alloy NO. 5315

- Pathway: 510(k) (Traditional)
- Applicant: Metalor Dental USA Corp.
- Decided: Dec 9, 1999 after 56 days
- Product code: EJS (Alloy, Other 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
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K024143: Aigis-Fine (2003), 0 descendants of its own

## Indications for use
Fabrication of Dental Crowns, Bridges, Inlays and Cast Partial-denture Frames.

Source page: https://510kreport.com/device/K993475
Methodology: https://510kreport.com/methodology