# K232676: Dental Porcelain Powder

- Pathway: 510(k) (Traditional)
- Applicant: Chengdu Besmile Medical Technology Co., Ltd.
- Decided: Jan 23, 2024 after 144 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: 1 generation back to K052710 (2006). 2 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K060441: Vita VM 7, Model NX77 XXXX, NX78XXXX, NX79 XXXX; Vita VM 8, Model VX60 XXXX, VX61 XXXX, VX62 XXXX; Vita VM 9, Model NX98, Vident (2006) Summary page 5.
- K052710: Vita VM7, Model NX77 XXXX, NX78XXXX, NX79 XXXX; Vita VM 8, Model VX60 XXXX, VX61 XXXX, VX62 XXXX; Vita VM 9,, Vident (2006) Summary page 5.

## Most influential descendants
- K250025: Porcelain Powder (Enamel/ Modifier,Stain/Glaze,Stain/Glaze-A,Modeling Fluid ) (2025), 0 descendants of its own

## Indications for use
This product is indicated for use as a veneering material for fixed prosthesis in crowns, bridges.

Source page: https://510kreport.com/device/K232676
Methodology: https://510kreport.com/methodology