Data / Medical devices / Netherlands / Light Tree Ventures Europe B.V.
Light Tree Ventures Europe B.V.: FDA-registered device maker in 'S-Gravenhage Zuid-Holland, Netherlands, 7 510(k) clearances
Light Tree Ventures Europe B.V. is registered with the FDA (registration 3017422691) in 'S-Gravenhage Zuid-Holland, Netherlands. It lists 4 device types. The FDA files 7 510(k) clearances under its listings, the newest dated May 12, 2026. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3017422691
- Address
- Saturnusstraat 95, 'S-Gravenhage Zuid-Holland, Netherlands, 2516 AG
- Owner or operator
- Light Tree Ventures Europe B.V. (10082702)
- Roles
- Complaint file establishment, Manufacturer, Specification developer
- First device listed
- September 20, 2021
- Registered through
- 2026
- Brand names listed
- BON Charge Red Light Toothbrush, BON Charge Red Light Toothbrush Refill, Bon Charge Red Light Face Mask, Bon Charge Red Light Face Mask Pro, DemarkQ WOW, DemarkQ POP, LUSTRE ClearSkin Renew Pro Facewear, Q-Rejuvalight Pro Facewear, Q-Renew LLLT Hair Growth Helmet and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Manufacturer | accessdata.fda.gov |
| Laser, Comb, Hair | OAP | 2 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Light Based Over The Counter Wrinkle Reduction | OHS | 2 | Complaint file establishment, Manufacturer, Specification developer | accessdata.fda.gov |
| Over-The-Counter Powered Light Based Laser For Acne | OLP | 2 | Complaint file establishment, 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 |
|---|---|---|---|---|---|---|
| May 12, 2026 | K260415 | myLEDmask 2 (MJ-144) | OHS | Substantially Equivalent | Light Tree Ventures Europe B.V. | accessdata.fda.gov |
| December 24, 2025 | K253349 | Hair Regrowth Cap (Model: T-119-HRC) | OAP | Substantially Equivalent | Light Tree Ventures Europe B.V. | accessdata.fda.gov |
| 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 |
| April 28, 2023 | K230042 | Q-Rejuvalight Pro Facewear (Model: P19-0023) | OHS | Substantially Equivalent | Light Tree Ventures Europe B.V. | accessdata.fda.gov |
| March 15, 2023 | K230124 | LUSTRE ClearSkin Renew Pro Facewear Mask(Model: PR4001) | 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 22, 2021 | K203214 | DemarkQ WOW, DemarkQ POP | OLP | Substantially Equivalent | Shenzhen Kaiyan Medical CO , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Over-The-Counter Powered Light Based Laser For Acne
- All makers of Light Based Over The Counter Wrinkle Reduction
- All makers of Laser, Comb, Hair
- All makers of Lamp, Infrared, Therapeutic Heating
Updated May 12, 2026. 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.