# K181868: SHINY RPL System

- Pathway: 510(k) (Traditional)
- Applicant: Ids, Ltd.
- Decided: Oct 5, 2018 after 85 days
- Product code: ONF (Powered Light Based Non-Laser Surgical Instrument With Thermal Effect)
- 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
Longest line of descent: 13 generations back to K910422 (1992). 114 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 116 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K102857: Ahwon's Ipl System, Ahwon Medi Instrument Co., Ltd. (2011) Summary page 4.

## Most influential descendants
- K220794: 10PL (2022), 0 descendants of its own

## Indications for use
The IDS SHINY IPL system is intended for use in Surgical, Aesthetic and Cosmetic applications in Dermatology by using filtered Intense Pulsed Light to treat the following conditions with different wavelengths to skin types I-IV. Wavelengths: Conditions: 415nm - 950nm Acne, Vulgaris 560nm - 950nm Melasma, Ephelides 640nm - 950nm Acne, Hair Reduction 640nm - 1200nm Hair Reduction 695nm - 1200nm Hair Reduction 755nm - 1200nm Hair Reduction

Source page: https://510kreport.com/device/K181868
Methodology: https://510kreport.com/methodology