Data / Medical devices / China / Shenzhen Chuangtong Yigou Technology Co., Ltd
Shenzhen Chuangtong Yigou Technology Co., Ltd: FDA-registered device maker in Shenzhen Guangdong, China, 3 510(k) clearances
Shenzhen Chuangtong Yigou Technology Co., Ltd is registered with the FDA (registration 3042254846) in Shenzhen Guangdong, China. It lists 4 device types. The FDA files 3 510(k) clearances under its listings, the newest dated August 7, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3042254846
- Address
- Room 2218, Rongchuang Zhihui Building A, Shangfen Community, Minzhi Street, Longhua District, Shenzhen Guangdong, China, 518109
- Owner or operator
- Shenzhen Chuangtong Yigou Technology Co., Ltd (10094129)
- Roles
- Manufacturer
- First device listed
- November 16, 2025
- Registered through
- 2026
- Brand names listed
- Hair Removal Device (Model: CT10, DT015, DT015 Pro, CTU05), Hair Removal Device/CT10, CT10 Pro, CT11, CT11 Pro, CT12, CT12 Pro, CTU05, CTU07, CTU09, CTU012, CTU015, CTU X, Hair Removal Device/DT015 Pro, DT015, DT017, DT017 Pro, DT025 Pro, DT025, Hand-held Hair Removal Device (Model: FZ-200A, FZ-201, FZ-202, CT05, CT06, CT07, CT08, CT09), LED Light Therapy Mask (Model: M01, M02, M03, M05, M06, M07, M08)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Manufacturer | accessdata.fda.gov |
| Light Based Over The Counter Wrinkle Reduction | OHS | 2 | Manufacturer | accessdata.fda.gov |
| Light Based Over-The-Counter Hair Removal | OHT | 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 |
|---|---|---|---|---|---|---|
| August 7, 2026 | K261601 | LED Light Therapy Mask (M01, M02, M03, M05, M06, M07, M08) | OHS | Substantially Equivalent | Shenzhen Chuangtong Yigou Technology Co., Ltd. | accessdata.fda.gov |
| March 11, 2026 | K254047 | Hair Removal Device (CT10, CT10 Pro, CT11, CT11 Pro, CT12, CT12 Pro, CTU05, CTU07, CTU09, CTU012, CTU015, CTU X, DT015 Pro, DT015, DT017 Pro, DT017, DT025 Pro, DT025) | OHT | Substantially Equivalent | Shenzhen Chuangtong Yigou Technology Co., Ltd. | accessdata.fda.gov |
| June 30, 2025 | K251000 | Hand-held Hair Removal Device (FZ-200A, FZ-201, FZ-202, CT05, CT06, CT07, CT08, CT09) | OHT | Substantially Equivalent | Shenzhen Chuangtong Yigou Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Light Based Over-The-Counter Hair Removal
- All makers of Light Based Over The Counter Wrinkle Reduction
- All makers of Lamp, Infrared, Therapeutic Heating
- All makers of Over-The-Counter Powered Light Based Laser For Acne
Updated August 7, 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.