Data / Medical devices / Catheter, Urethral / China
FDA-registered makers of Catheter, Urethral in China: 6 establishments
6 establishments in China are registered with the FDA to make Catheter, Urethral (product code GBM). 3 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Catheter, Urethral
- Product code
- GBM
- Country
- China
Makers of Catheter, Urethral in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Hangzhou Bever Medical Devices Co., Ltd. | Hangzhou Zhejiang, China | Specification developer | 2 | November 27, 2019 | 0 | 1 | 0 | api.fda.gov |
| Hangzhou Jimushi Meditech Co., Ltd. | Hangzhou Zhejiang, China | Manufacturer | 1 | June 1, 2020 | 0 | 0 | 0 | api.fda.gov |
| Well Lead Medical Co. Ltd | GUANGZHOU Guangdong, China | Manufacturer | 1 | March 5, 2025 | 0 | 0 | 0 | api.fda.gov |
| Integral Medical Products Co., Ltd. | SHAOXING Zhejiang, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Suzhou Jingle Polymer Medical Apparatus Co., Ltd. | SUZHOU Jiangsu, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Xianju Bever Medical Devices Co., Ltd. | Taizhou Zhejiang, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. 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.