Data / Medical devices / China / Shenzhen Light Tree Ventures Medical Technology Co.ltd
Shenzhen Light Tree Ventures Medical Technology Co.ltd: FDA-registered device maker in Shenzhen Guangdong, China, 5 510(k) clearances
Shenzhen Light Tree Ventures Medical Technology Co.ltd is registered with the FDA (registration 3030220360) in Shenzhen Guangdong, China. It lists 6 device types. The FDA files 5 510(k) clearances under its listings, the newest dated October 30, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3030220360
- Address
- Room 101, Building3, No. 40, Fuxin Street, Huaide Community Fuyong Street, Baoan District, Shenzhen, China, Shenzhen Guangdong, China, 518000
- Owner or operator
- Shenzhen Light Tree Ventures Medical Technology Co.LTD (10089226)
- Roles
- Exporter to the US
- First device listed
- November 16, 2023
- Registered through
- 2026
- Brand names listed
- Aduro light therapy Handheld, CeraThrive(TD-02), EnergyLounger, Neck & Decolletage LED, Neck and Decolletage Mask (Model: P23-0016/ZLD-50Y), Q-Rejuvalight Pro Facewear, Q-Renew LLLT Hair Growth Helmet (Q-HLMT-V1), QURE NECK AND DECOLLETAGE LED SYSTEM and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Fat Reducing Low Level Laser | OLI | 2 | Exporter to the US | accessdata.fda.gov |
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Exporter to the US | accessdata.fda.gov |
| Laser, Comb, Hair | OAP | 2 | Exporter to the US | accessdata.fda.gov |
| Light Based Over The Counter Wrinkle Reduction | OHS | 2 | Exporter to the US | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Exporter to the US | accessdata.fda.gov |
| Over-The-Counter Powered Light Based Laser For Acne | OLP | 2 | Exporter to the US | 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 |
|---|---|---|---|---|---|---|
| October 30, 2025 | K252414 | Q-Renew LLLT Hair Growth Helmet (Q-HLMT-V1) | OAP | Substantially Equivalent | Shenzhen Kaiyan Medical Equipment Co., Ltd. | accessdata.fda.gov |
| March 3, 2025 | K241947 | EnergyLounger (TY-01) | OHS | Substantially Equivalent | Shenzhen Kaiyan Medical Equipment Co., Ltd. | accessdata.fda.gov |
| April 28, 2023 | K230042 | Q-Rejuvalight Pro Facewear (Model: P19-0023) | OHS | Substantially Equivalent | Light Tree Ventures Europe B.V. | accessdata.fda.gov |
| December 20, 2022 | K221775 | LED Light Therapy Mask (model: MK-78, MK-04, MK66-H, MK66R-B, EL00003) | OHS | Substantially Equivalent | Light Tree Ventures Europe B.V. | accessdata.fda.gov |
| July 21, 2021 | K203271 | Aduro light therapy Handheld | OLP | Substantially Equivalent | Shenzhen Kaiyan Medical CO , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Light Based Over The Counter Wrinkle Reduction
- All makers of Fat Reducing Low Level Laser
- All makers of Lamp, Infrared, Therapeutic Heating
- All makers of Massager, Therapeutic, Electric
- All makers of Laser, Comb, Hair
- All makers of Over-The-Counter Powered Light Based Laser For Acne
Updated October 30, 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.