# K250413: Aglaia LED Beauty Device (BP-D2309)

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen Perfect Idea Technology Limited
- Decided: Mar 18, 2025 after 33 days
- Product code: OHS (Light Based Over The Counter Wrinkle Reduction)
- Device class: 2
- Regulation: 21 CFR 878.4810
- 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. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The Aglaia LED beauty device emits energy in the red and infrared light spectrum for the treatment of full face wrinkles and in the blue light spectrum for the treatment of mild to moderate acne.

Source page: https://510kreport.com/device/K250413
Methodology: https://510kreport.com/methodology