# Shenzhen Leaflife Technology Co., Ltd.

- Location (FDA's records): Shenzhen, CN
- FDA decisions: 7 (2020–2025): 7 510(k) clearances
- Product codes: GEX (3), OHT (2), QVJ (1), PBX (1)
- 510(k) review time since 2016: median 88 days, against 90 for FDA's reviews in the same codes and years (5 of 6 faster)
- Predicates its devices cite: 14 (2 its own); citations of its devices by later devices: 2 (2 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Medical Device Branch of Zhangzhou Easepal Industrial Co.,Lt: 2 (https://510kreport.com/company/medical-device-branch-of-zhangzhou-easepal-industrial-co-lt)
- Shandong Huamei Technology Co., Ltd.: 1 (https://510kreport.com/company/shandong-huamei-technology)
- Zhengzhou PZ Laser Slim Technology Co., Ltd.: 1 (https://510kreport.com/company/zhengzhou-pz-laser-slim-technology)
- Neauvia North America: 1 (https://510kreport.com/company/neauvia-north-america)
- Cartessa Aesthetics: 1 (https://510kreport.com/company/cartessa-aesthetics)
- Alma Lasers, Inc.: 1 (https://510kreport.com/company/alma-lasers)
- Wuhan Lotuxs Technology Co., Ltd.: 1 (https://510kreport.com/company/wuhan-lotuxs-technology)
- Shenzhen Goodwind Technology Development Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-goodwind-technology-development)

## Its most-cited devices
- K202980: Laser Therapy Device (2020), cited by 1
- K220103: LED Therapy Device (Planar LED/Planar LED mini) (2022), cited by 1

## Recent decisions
- K253219: LeafPure-Echo (LM-LPNdA) (Nov 25, 2025)
- K250916: WinForth (LM-E470KA) (Aug 14, 2025)
- K233760: Mjolnir Pro. (Multi–electrode plasma) (Feb 20, 2024)
- K230362: Planar LED mate (Sep 11, 2023)
- K220103: LED Therapy Device (Planar LED/Planar LED mini) (Apr 12, 2022)
- K212697: Leaf Smooth (Nov 19, 2021)
- K202980: Laser Therapy Device (Nov 19, 2020)

Source page: https://510kreport.com/company/shenzhen-leaflife-technology