Data / Medical devices / China / Acotec Scientific Co., Ltd.
Acotec Scientific Co., Ltd.: FDA-registered device maker in Beijing, China, 1 510(k) clearance
Acotec Scientific Co., Ltd. is registered with the FDA (registration 3015471899) in Beijing, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated October 7, 2025. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3015471899
- Address
- 4th, 5th Floor and North of 1st Floor, Building No.8, 16 Hongdabei Road, BDA, 100176 Beijing, China 10th Longqing Street, BDA, 100176 Beijing, China, Beijing, China, 100176
- Owner or operator
- Acotec Scientific Co.,Ltd. (10090931)
- Roles
- Manufacturer
- First device listed
- November 18, 2025
- Registered through
- 2027
- Brand names listed
- Cedar Endovenous Radiofrequency Catheters, Endovenous Radiofrequency Generator
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 |
|---|---|---|---|---|---|---|
| October 7, 2025 | K250688 | Cedar Endovenous Radiofrequency Catheter (ERA-C70-US); Cedar Endovenous Radiofrequency Catheter (ERA-C30-US); Endovenous Radiofrequency Generator (ERA-G5-US) | GEI | Substantially Equivalent | Acotec Scientific Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated October 7, 2025. 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.