Data / Medical devices / China / Shenzhen Leaflife Technology Co., Ltd.
Shenzhen Leaflife Technology Co., Ltd.: FDA-registered device maker in Shenzhen Guangdong, China, 7 510(k) clearances
Shenzhen Leaflife Technology Co., Ltd. is registered with the FDA (registration 3017954802) in Shenzhen Guangdong, China. It lists 5 device types. The FDA files 7 510(k) clearances under its listings, the newest dated November 25, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3017954802
- Address
- 4F,Bldg.C,JMDIndustrialPark,No.39QingfengBlvd.,BaolongIndustrial Area,LonggangDist.,Shenzhen,China, Shenzhen Guangdong, China, 518116
- Owner or operator
- Shenzhen Leaflife Technology Co., Ltd. (10079621)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- December 15, 2020
- Registered through
- 2026
- Brand names listed
- EPINIR, Korabeauticals Folliclear, LED Therapy Device, Laser Therapy Device, Leaf Smooth, LeafPure-Echo, Mjolnir Pro., Mjolnir Trio and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Light Based Over-The-Counter Hair Removal | OHT | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Low Power Electrosurgical Devices For Skin Lesion Destruction | QVJ | 2 | Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Massager, Vacuum, Radio Frequency Induced Heat | PBX | 2 | Manufacturer | accessdata.fda.gov |
| Powered Laser Surgical Instrument | GEX | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| November 25, 2025 | K253219 | LeafPure-Echo (LM-LPNdA) | GEX | Substantially Equivalent | Shenzhen Leaflife Technology Co., Ltd. | accessdata.fda.gov |
| August 14, 2025 | K250916 | WinForth (LM-E470KA) | PBX | Substantially Equivalent | Shenzhen Leaflife Technology Co., Ltd. | accessdata.fda.gov |
| February 20, 2024 | K233760 | Mjolnir Pro. (Multielectrode plasma) | QVJ | Substantially Equivalent | Shenzhen Leaflife Technology Co., Ltd. | accessdata.fda.gov |
| September 11, 2023 | K230362 | Planar LED mate | OHT | Substantially Equivalent | Shenzhen Leaflife Technology Co., Ltd. | accessdata.fda.gov |
| April 12, 2022 | K220103 | LED Therapy Device (Planar LED/Planar LED mini) | GEX | Substantially Equivalent | Shenzhen Leaflife Technology Co., Ltd. | accessdata.fda.gov |
| November 19, 2021 | K212697 | Leaf Smooth | OHT | Substantially Equivalent | Shenzhen Leaflife Technology Co., Ltd. | accessdata.fda.gov |
| November 19, 2020 | K202980 | Laser Therapy Device | GEX | Substantially Equivalent | Shenzhen Leaflife Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Light Based Over-The-Counter Hair Removal
- All makers of Powered Laser Surgical Instrument
- All makers of Low Power Electrosurgical Devices For Skin Lesion Destruction
- All makers of Massager, Therapeutic, Electric
- All makers of Massager, Vacuum, Radio Frequency Induced Heat
Updated November 25, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.