# K042888: Demetron Ids Curing Light

- Pathway: 510(k) (Traditional)
- Applicant: Kerr Corp.
- Decided: Nov 10, 2004 after 22 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.
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. The FDA summary names its predicate without a number.
- (no number) L.E. Demetron: named in the summary without a submission number

## Indications for use
The Demetron 1.D.S. is a L.E.D. visible light curing unit intended for polymerization of light cure materials by dental professionals.

Source page: https://510kreport.com/device/K042888
Methodology: https://510kreport.com/methodology