Data / Medical devices / China / Beijing Taktvoll Technology Co., Ltd.
Beijing Taktvoll Technology Co., Ltd.: FDA-registered device maker in Beijing, China, 1 510(k) clearance
Beijing Taktvoll Technology Co., Ltd. is registered with the FDA (registration 3027988352) in Beijing, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 23, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3027988352
- Address
- Room 302, Floor 3, Building 10, No. 13A, Jingsheng South 4th Street, Jinqiao Science and Technology Industrial Base, Tongzhou District, Beijing, Beijing, China, 100012
- Owner or operator
- Beijing Taktvoll Technology Co., Ltd. (10092426)
- Roles
- Manufacturer
- First device listed
- January 6, 2025
- Registered through
- 2026
- Brand names listed
- electrosurgical unit ES-100,ES-300,ES-300D,ES-300S,ES-300 PLUS,ES-200 PLUS,ES-200PK,ES-100 PLUS,ES-120LEEP;
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Electrosurgical, Cutting & Coagulation & Accessories | GEI | 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 |
|---|---|---|---|---|---|---|
| December 23, 2024 | K240975 | Electrosurgical Generator (ES-100); Electrosurgical Generator (ES-300) | GEI | Substantially Equivalent | Beijing Taktvoll Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated December 23, 2024. 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.