# K022862: Transcure, Model 2910

- Pathway: 510(k) (Traditional)
- Applicant: Kinetic Instruments, Inc.
- Decided: Oct 18, 2002 after 51 days
- Product code: EBZ (Activator, Ultraviolet, For Polymerization)
- Device class: 2
- Regulation: 21 CFR 872.6070
- 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
- K052122: Bisco Led (2006), 0 descendants of its own

## Indications for use
Light Activation System for Dental Restorative Resins Visible Inspection of the Oral Cavity

Source page: https://510kreport.com/device/K022862
Methodology: https://510kreport.com/methodology