Data / Medical devices / China / Shenzhen Jianchao Intelligent Technology Co., Ltd.
Shenzhen Jianchao Intelligent Technology Co., Ltd.: FDA-registered device maker in Shenzhen Guangdong, China, 5 510(k) clearances
Shenzhen Jianchao Intelligent Technology Co., Ltd. is registered with the FDA (registration 3030234086) in Shenzhen Guangdong, China. It lists 4 device types. The FDA files 5 510(k) clearances under its listings, the newest dated August 10, 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
- 3030234086
- Address
- Rm101, 201, 301, Bldg.25, No.68 Hexiu West Road, Fuhai St., Baoan, Shenzhen Guangdong, China, 518103
- Owner or operator
- Shenzhen Jianchao Intelligent Technology Co., Ltd. (10089295)
- Roles
- Foreign private label distributor, Manufacturer
- First device listed
- November 27, 2023
- Registered through
- 2026
- Brand names listed
- Dreame Nova IPL Home Use Hair Removal Device (Model: R3C16-G Pro), Facial & Body Beauty Device, Facial & Body Beauty Device (Models: F2210 Pro, F5808, INIA-ED001, INIA-ED002, INIA-BLD001, E1507), Facial & Body Beauty Device (Models: INIA-BD002, INIA-BD003, INIA-BD004, F2C15, F3222 Pro, F5516), GlowPop Facial & Body Beauty Device (Model: F3606), GlowPop Facial & Body Beauty Device (model: F3606), Hair Removal Device (Model: R3C16-V Pro), Hair Removal Device, Model(s): R2815-G Pro, R2815-G and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Light Based Over The Counter Wrinkle Reduction | OHS | 2 | Foreign private label distributor, 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 | Foreign private label distributor, Manufacturer | accessdata.fda.gov |
| Stimulator, Transcutaneous Electrical, Aesthetic Purposes | NFO | 2 | Foreign private label distributor, 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 10, 2026 | K261705 | Hair Removal Device (R3C16-G Pro, R3C16-V Pro) | OHT | Substantially Equivalent | Shenzhen Jianchao Intelligent Technology Co., Ltd. | accessdata.fda.gov |
| January 30, 2026 | K253833 | Facial & Body Beauty Device (model: INIA-BD001, INIA-BD002, INIA-BD003, INIA-BD004, F2C15, F3222 Pro, F5516, F3606, F2210 Pro, F5808, INIA-ED001, INIA-ED002, INIA-BLD001, E1507) | OHS | Substantially Equivalent | Shenzhen Jianchao Intelligent Technology Co., Ltd. | accessdata.fda.gov |
| October 9, 2025 | K252553 | Facial & Body Beauty Device (INIA-BD001, INIA-BD002, INIA-BD003, INIA-BD004, F2C15, F3222 Pro, F5516, F3606, F2210 Pro, F5808, INIA-ED001, INIA-ED002, INIA-BLD001, E1507) | NFO | Substantially Equivalent | Shenzhen Jianchao Intelligent Technology Co., Ltd. | accessdata.fda.gov |
| December 6, 2024 | K242710 | Hair Removal Device (R3C16-P, R3C16-W, R3C16-G, R3C16-P Pro, R3C16-W Pro, R3C16-G Pro, R3505-W, R3505-B, R3505-W Pro, R3505-B Pro) | OHT | Substantially Equivalent | Shenzhen Jianchao Intelligent Technology Co., Ltd. | accessdata.fda.gov |
| November 20, 2023 | K232575 | Hair Removal Device, Model(s): R2815-G Pro, R2815-G | OHT | Substantially Equivalent | Shenzhen Jianchao Intelligent 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 Stimulator, Transcutaneous Electrical, Aesthetic Purposes
- All makers of Over-The-Counter Powered Light Based Laser For Acne
Updated August 10, 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.