# K252911: Lux HD 2530 detector (Lux HD 2530)

- Pathway: 510(k) (Special)
- Applicant: Iray Imaging Technology (Haining) Limited
- Decided: Oct 9, 2025 after 27 days
- Product code: MQB (Solid State X-Ray Imager (Flat Panel/Digital Imager))
- Device class: 2
- Regulation: 21 CFR 892.1680
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 17 generations back to K981556 (1998). 28 ancestors in all.
No later device cites it as a predicate yet.
0 of 29 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K243556: Lux HD 35 Detector (Lux HD 35); Lux HD 43 Detector (Lux HD 43), Iray Imaging Technology (Haining) Limited (2025) Summary page 6.

## Indications for use
Lux HD 2530 Detector is indicated for digital imaging solutions designed to provide general radiographic diagnosis for human anatomy including both adult and pediatric patients. It is intended to replace film/screen systems in all general–purpose diagnostic procedures. Lux HD 2530 Detector is not intended for mammography or dental applications.

Source page: https://510kreport.com/device/K252911
Methodology: https://510kreport.com/methodology
