Manufacturer and brand owner in Wuhan, Hubei, China. 2 device types, 1 product catalogued, 2 clearances.
Ankon Technologies Co., Ltd. is a contract manufacturer holding a current FDA establishment registration. The registration covers Magnetically Maneuvered Capsule Endoscopy System, System, Imaging, Gastrointestinal, Wireless, Capsule. 1 of its products is catalogued under its own name. Its earliest product listing with the FDA dates from 2020.
Registration
FDA registration record for Ankon Technologies Co., Ltd. | Registered name | ANKON TECHNOLOGIES CO., LTD. |
| Status | Registered |
| Registration expires | 2026 |
| Registration number | 3017400296 |
| FEI number | 3017400296 |
| DUNS | 549329633 |
| Establishment type | Contract manufacturer, Manufacturer |
Chinese Registration
Chinese company register details for Ankon Technologies Co., Ltd. | Chinese legal name | 安翰科技（武汉）股份有限公司 |
| Unified social credit code | 914201006953078688 |
| Source | NMPA UDI database |
Location
Address of Ankon Technologies Co., Ltd. | City | Wuhan |
| Province | Hubei |
| Address | No. 666, Hi-tech Road, East Lake New Technology Development Zone |
| Postal code | 430073 |
| Country | China |
From the Company
Published by the company on its own website, not by the FDA.
Information published by Ankon Technologies Co., Ltd. | Founded | 2009 |
| Main products | Magnetic-controlled capsule gastroscopy system |
| Certifications | CE, FDA De Novo, NMPA |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.