# K052710: Vita VM7, Model NX77 XXXX, NX78XXXX, NX79 XXXX; Vita VM 8, Model VX60 XXXX, VX61 XXXX, VX62 XXXX; Vita VM 9,

- Pathway: 510(k) (Special)
- Applicant: Vident
- Decided: Jan 13, 2006 after 106 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
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K232676: Dental Porcelain Powder (2024), 1 descendant of its own
- K250025: Porcelain Powder (Enamel/ Modifier,Stain/Glaze,Stain/Glaze-A,Modeling Fluid ) (2025), 0 descendants of its own

## Indications for use
Vita VM®porcelains are indicated for use as a veneering material for fixed prosthesis in crowns, bridges, and dental implant abutments. These devices are used in prosthetic dentistry by forming a porcelain veneer on to a ceramic or metal substructure into the shape of a dental crown. For use by or on the order of a dental professional such as DDS or DMD. Not for use by the general public or OTC.

Source page: https://510kreport.com/device/K052710
Methodology: https://510kreport.com/methodology