Data / Medical devices / China / Haidari Beauty Technology (beijing) Co., Ltd
Haidari Beauty Technology (beijing) Co., Ltd: FDA-registered device maker in Beijing, China, 1 510(k) clearance
Haidari Beauty Technology (beijing) Co., Ltd is registered with the FDA (registration 3023850562) in Beijing, China. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 3, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3023850562
- Address
- Room 110, Building 1, No.18, Jingxing Street, Nanshao Town, Changping District, Beijing, China, 102299
- Owner or operator
- Haidari Beauty Technology (Beijing) Co., Ltd (10095703)
- Roles
- Manufacturer
- First device listed
- April 16, 2026
- Registered through
- 2026
- Brand names listed
- CO2 Laser Treatment Machine-CO2 CFR1M1, CO2 Laser Treatment Machine-CO2 CFR1M2, CO2 Laser Treatment Machine-CO2 CFR2H1, CO2 Laser Treatment Machine-CO2 CFR2H2, CO2 Laser Treatment Machine-CO2 CFR2M1, CO2 Laser Treatment Machine-CO2 CFR3H1, CO2 Laser Treatment Machine-CO2 CFR3H2, CO2 Laser Treatment Machine-CO2 CFR3M1 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Brush, Dermabrasion, Powered | GFE | 1 | Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Manufacturer | accessdata.fda.gov |
| Powered Laser Surgical Instrument | GEX | 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 |
|---|---|---|---|---|---|---|
| March 3, 2026 | K253920 | CO2 Laser Treatment Machine (CFR3M1) | GEX | Substantially Equivalent | Haidari Beauty Technology (Beijing) Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Massager, Therapeutic, Electric
- All makers of Brush, Dermabrasion, Powered
- All makers of Powered Laser Surgical Instrument
Updated March 3, 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.