# K071251: DEMI

- Pathway: 510(k) (Traditional)
- Applicant: Kerr Corporation
- Decided: Jul 26, 2007 after 83 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.
2 later devices descend from it; 1 cites it directly.
0 of 3 devices 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 II: named in the summary without a submission number

## Most influential descendants
- K123468: Demi Ultra (2013), 1 descendant of its own
- K163064: Demi Ultra (2017), 0 descendants of its own

## Indications for use
The Demi is an L.E.D. visible light curing unit intended for polymerization of light cure materials by dental professionals.

Source page: https://510kreport.com/device/K071251
Methodology: https://510kreport.com/methodology