Ankon Medical Technologies (Shanghai) Co., Ltd.
Registered establishment in Shanghai, China. 2 device types.
Ankon Medical Technologies (Shanghai) Co., Ltd. is a contract manufacturer holding a current FDA establishment registration. The registration covers System, Gastrointestinal Motility (Electrical), Magnetically Maneuvered Capsule Endoscopy System. Its earliest product listing with the FDA dates from 2020.
Registration
| Registered name | ANKON MEDICAL TECHNOLOGIES (SHANGHAI) CO., LTD. |
|---|---|
| Status | Registered |
| Registration expires | 2026 |
| Registration number | 3015198783 |
| FEI number | 3015198783 |
| Establishment type | Contract manufacturer, Manufacturer |
Location
| City | Shanghai |
|---|---|
| Province | Shanghai |
| Address | F 3 |
| Postal code | 201206 |
| Country | China |
What It Makes
| Device type | Class | Listed under the names | Listed since | Chinese makers |
|---|---|---|---|---|
| Magnetically Maneuvered Capsule Endoscopy System | Class 2 | NaviCam Xpress Stomach Capsule Endoscope System (NaviCam Xpress Stomach System), NaviCam Tether, NaviCam Stomach Capsule and NaviCam Tether | 2021 | 2 |
| System, Gastrointestinal Motility (Electrical) | Class 2 | IntraMarX Radiopaque Markers AGIROMC1-1, IntraMarX 3D Radiopaque Markers | 2020 | 1 |
From the Company
Published by the company on its own website, not by the FDA.
| Main products | magnetically controlled capsule endoscopy system |
|---|---|
| Certifications | CFDA Class III |
Nearby Manufacturers
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.
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