Data / Medical devices / China / Beijing Huacheng Taike Technology Co., Ltd.
Beijing Huacheng Taike Technology Co., Ltd.: FDA-registered device maker in Beijing, China, 3 510(k) clearances
Beijing Huacheng Taike Technology Co., Ltd. is registered with the FDA (registration 3019559090) in Beijing, China. It lists 1 device type. The FDA files 3 510(k) clearances under its listings, the newest dated February 27, 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
- 3019559090
- Address
- Room 402, 4th Floor, Building 4, Courtyard 5, South Third Street, Huoxian Town, Tongzhou District 101113Beijing,P.R.China, Beijing, China, 101113
- Owner or operator
- Beijing HuaCheng Taike Technology Co., Ltd. (10085432)
- Roles
- Manufacturer
- First device listed
- June 16, 2022
- Registered through
- 2026
- Brand names listed
- Dermatological Diode Laser Systems, Medical Alexandrite and Nd:YAG laser Therapy System (CM11LP), Medical Ultra-Pico Laser Treatment System (CM-SP-1064&532)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| 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 |
|---|---|---|---|---|---|---|
| February 27, 2026 | K253829 | Medical Ultra-Pico Laser Treatment System (CM-SP-1064&532) | GEX | Substantially Equivalent | Beijing HuaCheng Taike Technology Co., Ltd. | accessdata.fda.gov |
| February 27, 2026 | K253828 | Medical Alexandrite and Nd:YAG laser Therapy System (CM11LP) | GEX | Substantially Equivalent | Beijing HuaCheng Taike Technology Co., Ltd. | accessdata.fda.gov |
| April 26, 2021 | K210663 | Dermatological Diode Laser Systems | GEX | Substantially Equivalent | Beijing HuaCheng Taike Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated February 27, 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.