# K201856: Provicol QM Aesthetic

- Pathway: 510(k) (Special)
- Applicant: Voco GmbH
- Decided: Aug 26, 2020 after 51 days
- Product code: EMA (Cement, Dental)
- Device class: 2
- Regulation: 21 CFR 872.3275
- 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
Provicol QM Aesthetic is intended for use as: – Temporary luting of temporary restorations (crowns, bridges, inlays and onlays) – Temporary luting of permanent restorations (crowns, bridges, inlays and onlays)

Source page: https://510kreport.com/device/K201856
Methodology: https://510kreport.com/methodology