# K122995: Intense Pulsed Light (Ipl) Systems

- Pathway: 510(k) (Traditional)
- Applicant: Beijing Kes Biology Technology Co., Ltd.
- Decided: Jan 22, 2013 after 118 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: 11 generations back to K910422 (1992). 90 ancestors in all.
16 later devices descend from it; 7 cite it directly.
0 of 107 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K093627: Ipulselight Ipl System, Models HS 300C and HS 650, Shanghai Apolo Medical Technologies Co., Ltd. (2011) Summary page 2.

## Most influential descendants
- K161286: IPL Therapy Machine (2016), 5 descendants of its own
- K192521: Intense Pulsed Light Treatment System (2019), 3 descendants of its own
- K131859: Multifunctional Series (2013), 3 descendants of its own
- K192519: Multi-modality workstation (2019), 2 descendants of its own
- K140668: Platinumgmt Ipl System Cloud (2014), 2 descendants of its own

## Indications for use
The Intense Pulsed Light (IPL) Systems (inclusive of the handpiece used to deliver pulsed-light energy) are indicated for use in surgical, aesthetic and cosmetic applications in permanent hair removal, skin rejuvenation, reduction of pigmented lesions, acne therapy, freckle, vascular lesions and facial blemish removal.

Source page: https://510kreport.com/device/K122995
Methodology: https://510kreport.com/methodology