# K262074: Any-Zircos

- Pathway: 510(k) (Traditional)
- Applicant: Mediclus Co., Ltd.
- Decided: Aug 21, 2026 after 60 days
- Product code: EIH (Powder, Porcelain)
- Device class: 2
- Regulation: 21 CFR 872.6660
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 11 generations back to K830955 (1983). 27 ancestors in all.
No later device cites it as a predicate yet.
0 of 28 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K241151: Luxen 5G, Dentalmax Co., Ltd. (2024) Summary page 5.
- K171585: LUXEN Zr, LUXEN Smile, Dentalmax Co., Ltd. (2018) Summary page 5.

## Indications for use
Any-Zircos is indicated for the production of inlays or onlays, 3-unit bridges and full crowns.

Source page: https://510kreport.com/device/K262074
Methodology: https://510kreport.com/methodology