Data / Medical devices / India / Light Tree Technology India Private Limited
Light Tree Technology India Private Limited: FDA-registered device maker in Gurugram Haryana, India, 3 510(k) clearances
Light Tree Technology India Private Limited is registered with the FDA (registration 3018949797) in Gurugram Haryana, India. It lists 3 device types. The FDA files 3 510(k) clearances under its listings, the newest dated December 24, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3018949797
- Address
- Building No.-GP47, Sector-18 Maruti Industrial Area, Gurugram Haryana, India, 122008
- Owner or operator
- Light Tree Technology India Private Limited (10081695)
- Roles
- Complaint file establishment, Manufacturer
- First device listed
- May 7, 2021
- Registered through
- 2026
- Brand names listed
- Beauty Pie ALL System Grow H-Wave LED & Scalp Treatment, Light Doctor 15W handheld
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Laser, Comb, Hair | OAP | 2 | Manufacturer | accessdata.fda.gov |
| Over-The-Counter Powered Light Based Laser For Acne | OLP | 2 | 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 |
|---|---|---|---|---|---|---|
| December 24, 2025 | K253349 | Hair Regrowth Cap (Model: T-119-HRC) | OAP | Substantially Equivalent | Light Tree Ventures Europe B.V. | accessdata.fda.gov |
| November 20, 2024 | K242363 | HIGHERDOSE Red Light Hat (HG-120K) | OAP | Substantially Equivalent | Shenzhen Kaiyan Medical Equipment Co., Ltd. | accessdata.fda.gov |
| April 28, 2023 | K230597 | Aduro Comb (Model: SZ-22, SZ-22A, SZ-22B) | OAP | Substantially Equivalent | Light Tree Ventures Europe B.V. | accessdata.fda.gov |
Compare with other makers
- All makers of Over-The-Counter Powered Light Based Laser For Acne
- All makers of Laser, Comb, Hair
- All makers of Lamp, Infrared, Therapeutic Heating
Updated December 24, 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.