# Hangzhou Jimushi Meditech Co., Ltd.

- Location (FDA's records): Hangzhou, CN
- FDA decisions: 3 (2020–2026): 3 510(k) clearances
- Product codes: EZD (2), GBM (1)
- 510(k) review time since 2016: median 138 days, against 214 for FDA's reviews in the same codes and years (3 of 3 faster)
- Predicates its devices cite: 3 (2 its own); citations of its devices by later devices: 3 (2 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
- Teleflexmedical, Inc.: 1 (https://510kreport.com/company/teleflexmedical)

## Firms that cite its devices most
- Chengdu Daxan Innovative Medical Tech. Co., Ltd.: 1 (https://510kreport.com/company/chengdu-daxan-innovative-medical-tech)

## Its most-cited devices
- K200134: Jimushi Sterile Urethral Catheter for single use (2020), cited by 3

## Recent decisions
- K260394: Hydrophilic coated intermittent nalaton catheter for single use-ready to use (NCR) (Jun 24, 2026)
- K222677: Intermittent nelaton catheter for single use (Apr 5, 2023)
- K200134: Jimushi Sterile Urethral Catheter for single use (Jun 1, 2020)

Source page: https://510kreport.com/company/hangzhou-jimushi-meditech