# K061823: Admira Protect/Admira Protect Single Dose

- Pathway: 510(k) (Special)
- Applicant: Voco GmbH
- Decided: Jul 21, 2006 after 23 days
- Product code: EBC (Sealant, Pit And Fissure, And Conditioner)
- Device class: 2
- Regulation: 21 CFR 872.3765
- 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
treatment of hypersensitive dentine treatment of cervical areas (including crown margins, after tooth cleaning or tartar removal, exposed cervical areas etc.)

Source page: https://510kreport.com/device/K061823
Methodology: https://510kreport.com/methodology