# K051780: Jetlite 5000

- Pathway: 510(k) (Traditional)
- Applicant: J. Morita USA, Inc.
- Decided: Jul 28, 2005 after 27 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.
8 later devices descend from it; 1 cites it directly.
0 of 9 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 no predicate by number.

## Most influential descendants
- K063529: Pencure, Model VL-7 (2007), 7 descendants of its own
- K071190: Root ZX II (2007), 6 descendants of its own
- K090925: Multiple (Apex Locator), Model RCM-7 (2009), 2 descendants of its own
- K151274: Dr's Finder (2016), 1 descendant of its own
- K112665: Tri Auto Mini - Endodeontic Treatment Motorized Handpiece (2012), 1 descendant of its own

## Indications for use
The Jetlite 5000 is intended to polymerize (set) resinous dental pit and fissure sealants or dental restorative materials by transmission of light through a rod.

Source page: https://510kreport.com/device/K051780
Methodology: https://510kreport.com/methodology