# K140668: Platinumgmt Ipl System Cloud

- Pathway: 510(k) (Traditional)
- Applicant: Global Medical Technology S.L.
- Decided: Dec 19, 2014 after 276 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). 92 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 95 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K131859: Multifunctional Series, Beijing Honkon Technologies Co., Ltd. (2013) Summary page 5.
- K122995: Intense Pulsed Light (Ipl) Systems, Beijing Kes Biology Technology Co., Ltd. (2013) Summary page 5.

## Most influential descendants
- K153717: Venus Versa System (2016), 1 descendant of its own
- K232192: Venus Versa PRO System (2023), 0 descendants of its own

## Indications for use
The PlatinumGMT™ IPL System Cloud device (inclusive of the hand piece used to deliver pulsed-light energy) is indicated for use in surgical, aesthetic and cosmetic applications in permanent hair reduction, moderate inflammatory acne vulgaris, benign cutaneous pigmented and vascular lesions. Permanent hair reduction is defined as the long-term stable reduction in the number of hairs regrowing when measured at 6, 9, and 12 months after the completion of a treatment regimen.

Source page: https://510kreport.com/device/K140668
Methodology: https://510kreport.com/methodology