Data / Medical devices / China / Dreame Trading (tianjin) Co., Ltd.
Dreame Trading (tianjin) Co., Ltd.: FDA-registered device maker in Tianjin, China, 3 510(k) clearances
Dreame Trading (tianjin) Co., Ltd. is registered with the FDA (registration 3044572954) in Tianjin, China. It lists 4 device types. The FDA files 3 510(k) clearances under its listings, the newest dated February 23, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3044572954
- Address
- Room 2112-1-1, South District, Finance and Trade Center, No.6975 Yazhou Road, Dongjiang Bonded Port Area Tianjin Pilot Free Trade Zone, Tianjin, China, 300463
- Owner or operator
- Dreame Trading (Tianjin) Co., Ltd. (10095569)
- Roles
- Exporter to the US, Foreign private label distributor
- First device listed
- March 31, 2026
- Registered through
- 2026
- Brand names listed
- DREAME Astra IPL Hair Removal Device/Model:T32A, Dreame Chrona Photon Anti-Aging Skincare Mask/Model: RB-053(AB01A), Dreame Chrona Pro Photon Anti-Aging Neck Beauty Device/Model: RB-053(AB01P), Dreame Chrona Pro Photon Neck Beauty Device/Model:AB02A, Dreame Nova Hair Removal Device/model:R3C16-G Pro
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Exporter to the US, Foreign private label distributor | accessdata.fda.gov |
| Light Based Over The Counter Wrinkle Reduction | OHS | 2 | Exporter to the US, Foreign private label distributor | accessdata.fda.gov |
| Light Based Over-The-Counter Hair Removal | OHT | 2 | Exporter to the US, Foreign private label distributor | accessdata.fda.gov |
| Over-The-Counter Powered Light Based Laser For Acne | OLP | 2 | Exporter to the US, Foreign private label distributor | 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 |
|---|---|---|---|---|---|---|
| February 23, 2026 | K253666 | IPL Hair Removal Device (Models: T31A, T32A) | OHT | Substantially Equivalent | Shenzhen Mlay Intelligent Technology Co., Ltd. | accessdata.fda.gov |
| January 23, 2026 | K253712 | LED Light Therapy Mask (RB-051, RB-061, RB-071, RB-052, RB-062, RB-072, RB-053, RB-063, RB-073) | OHS | Substantially Equivalent | Shenzhen Rainbow 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 |
Compare with other makers
- All makers of Light Based Over-The-Counter Hair Removal
- All makers of Over-The-Counter Powered Light Based Laser For Acne
- All makers of Lamp, Infrared, Therapeutic Heating
- All makers of Light Based Over The Counter Wrinkle Reduction
Updated February 23, 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.