# Ankon Technologies Co., Ltd.

- Location (FDA's records): Wuhan, CN
- FDA decisions: 2 (2022–2023): 1 510(k) clearance and 1 De Novo grant
- Product codes: NEZ (1), QZF (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Given Imaging, Ltd.: 1 (https://510kreport.com/company/given-imaging)

## Firms that cite its devices most
- Digestaid - Artificial Intelligence Development SA: 1 (https://510kreport.com/company/digestaid-artificial-intelligence-development)
- CapsoVision, Inc.: 1 (https://510kreport.com/company/capsovision)

## Its most-cited devices
- DEN230027: NaviCam ProScan (2023), cited by 2

## Recent decisions
- DEN230027: NaviCam ProScan (Dec 12, 2023)
- K221590: NaviCam Small Bowel Capsule Endoscopy System (Dec 2, 2022)

Source page: https://510kreport.com/company/ankon-technologies