# K133007: DX3000-L

- Pathway: 510(k) (Special)
- Applicant: Dexcowin Co., Ltd.
- Decided: Apr 24, 2014 after 211 days
- Product code: MUH (System, X-Ray, Extraoral Source, Digital)
- Device class: 2
- Regulation: 21 CFR 872.1800
- 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. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K173046: Cocoon Portable Handheld X-Ray System (2017), 1 descendant of its own
- K250687: Cocoon Solo (DX-7020s) (2025), 0 descendants of its own

## Indications for use
DX3000 is a portable x-ray system indicated for taking diagnostic dental x-rays for both pediatric and adult patients using inirsorsi film or digital seasors

Source page: https://510kreport.com/device/K133007
Methodology: https://510kreport.com/methodology