# K111321: Remote View Software

- Pathway: 510(k) (Special)
- Applicant: Cariescan, Ltd.
- Decided: May 17, 2011 after 6 days
- Product code: NBL (Light-Induced Fluorescence Caries Detector )
- Device class: 2
- Regulation: 21 CFR 872.1745
- 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
For use by dental professionals as an aid in the diagnosis and monitoring of dental caries.

Source page: https://510kreport.com/device/K111321
Methodology: https://510kreport.com/methodology