# K021083: Veracam

- Pathway: 510(k) (Traditional)
- Applicant: Lumalite, Inc.
- Decided: Aug 30, 2002 after 149 days
- Product code: EIA (Unit, Operative Dental)
- Device class: 1
- Regulation: 21 CFR 872.6640
- 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
- K040116: Hawk Intraoral Camera and Accessories (2004), 0 descendants of its own

## Indications for use
The intraaal camera system, Veracam, of Lumalite, Inc. is used to provide a view of the mouth so that it assists the dentist in describing dental procedures and to show a patient a before view and an after view of his mouth in order to show the patient results of the dental prqcedures which the dentist has performed on him

Source page: https://510kreport.com/device/K021083
Methodology: https://510kreport.com/methodology