# K050362: Vita PM 7 (20 Gram Bottles), Vita PM 7 (50 Gram Bottles)

- Pathway: 510(k) (Traditional)
- Applicant: Vident
- Decided: Mar 15, 2005 after 29 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.
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
- K193436: VITA Ambria (2020), 0 descendants of its own

## Indications for use
Vita PM7 pressable ceramic is to be used for the fabrication of Single and multi-surface inlays Onlays Veneers Partial crowns Anterior crowns Premolar crowns Also for oxide-ceramic crown and bridge substructures to be veneered with conventional porcelain. 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/K050362
Methodology: https://510kreport.com/methodology