Beijing Huacheng Taike Technology Co., Ltd.
Beijing, CN
BEIJING HUACHENG TAIKE TECHNOLOGY CO., LTD. appears in FDA device records in Beijing, CN. FDA records list 3 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 3 510(k) clearances for Beijing Huacheng Taike Technology Co., Ltd. between 2021 and 2026. The busiest year on record is 2026, with 2. The most recent is 2026, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2021 | 1 |
| 2026 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K253829 | Medical Ultra-Pico Laser Treatment System (CM-SP-1064&532) | GEX | Substantially Equivalent | |
| K253828 | Medical Alexandrite and Nd:YAG laser Therapy System (CM11LP) | GEX | Substantially Equivalent | |
| K210663 | Dermatological Diode Laser Systems | GEX | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3019559090 | 3019559090 | BEIJING HUACHENG TAIKE TECHNOLOGY CO., LTD. | Room 402, 4th Floor, Building 4, Courtyard 5, South Third Street, Huoxian Town, Tongzhou District, Beijing 101113 CN | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain