# K102857: Ahwon's Ipl System

- Pathway: 510(k) (Traditional)
- Applicant: Ahwon Medi Instrument Co., Ltd.
- Decided: Jan 14, 2011 after 107 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: 12 generations back to K910422 (1992). 113 ancestors in all.
2 later devices descend from it; 2 cite 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)
- K091664: GSD Intense Pulsed Light System, Models: GP666C4, GP666C, Shenzhen Gsd Tech Co., Ltd. (2009) Summary page 1.
- K090837: Stratapulse TS and Stratapulse, Advanced Medical Photonics (2009) Summary page 1.

## Most influential descendants
- K181868: SHINY RPL System (2018), 1 descendant of its own
- K220794: 10PL (2022), 0 descendants of its own

## Indications for use
The Ahwon RPL, R2PL system intended ui e for in Surgical, Asthetic and Cosmetic Application in Dermatology by using filtered Intense Pulsed Light to treat the following conditions with different wavelengths to skin types I-IV: Model RPL: 560-1200nm — Melasma, Ephelides 590-1200nm — Port wine stains, Rosacea 640-1200nm — Melasma, 695-1200nm — Hair reduction/removal, Vascular lesions. Model R2PL: 415-950n — Acne, vulgaris, 560-950nm — Melasma, Ephelides 590-950nm — Port wine stains, Rosacea 640-1200nm — Melasma, 695-1200nm — Hair reduction/Removal, Vascular lesions.

Source page: https://510kreport.com/device/K102857
Methodology: https://510kreport.com/methodology