# K093446: Vita VMK Master

- Pathway: 510(k) (Special)
- Applicant: Vita Zahnfabrik H. Rauter GmbH & Co. Kg.
- Decided: Dec 3, 2009 after 28 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.
No later device cites it as a predicate yet.
0 of 1 device 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.

## Indications for use
Vita VMK Master® is indicated for use as part of a dental restoration in the form of a ceramic veneering material (full or partial) of a metal substructure. For use by or on the order of a dental professional such as DOS or DMD. Not for use by the general public or OTC.

Source page: https://510kreport.com/device/K093446
Methodology: https://510kreport.com/methodology