Data / Medical devices / Hemostatic Metal Clip For The Gi Tract / China
FDA-registered makers of Hemostatic Metal Clip For The Gi Tract in China: 13 establishments
13 establishments in China are registered with the FDA to make Hemostatic Metal Clip For The Gi Tract (product code PKL). 13 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Hemostatic Metal Clip For The Gi Tract
- Product code
- PKL
- Country
- China
Makers of Hemostatic Metal Clip For The Gi Tract in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Micro-Tech (Nanjing) Co., Ltd. | Nanjing Jiangsu, China | Manufacturer | 8 | September 8, 2025 | 0 | 0 | 0 | api.fda.gov |
| Micro-Tech (Nanjing) Co., Ltd. | NAN JING Jiangsu, China | Manufacturer | 8 | September 8, 2025 | 0 | 0 | 0 | api.fda.gov |
| Hangzhou AGS MedTech Co., Ltd. | Hangzhou Zhejiang, China | Manufacturer, Repackager or relabeler | 6 | August 10, 2026 | 0 | 0 | 0 | api.fda.gov |
| Anrei Medical (Hangzhou) Co., Ltd. | HANGZHOU Zhejiang, China | Manufacturer | 2 | October 2, 2026 | 0 | 0 | 0 | api.fda.gov |
| Zhejiang Chuangxiang Medical Technology Co., Ltd. | Hangzhou Zhejiang, China | Contract manufacturer, Manufacturer | 2 | May 27, 2022 | 0 | 0 | 0 | api.fda.gov |
| Alton Shanghai Medical Instruments Co Ltd | Shanghai, China | Manufacturer | 1 | January 11, 2024 | 0 | 0 | 0 | api.fda.gov |
| Beijing ZKSK Technology Co., Ltd. | beijing, China | Manufacturer | 1 | November 14, 2022 | 0 | 0 | 0 | api.fda.gov |
| Jiangxi Zhuoruihua Medical Instrument Co., Ltd. | Ji 'an Jiangxi, China | Manufacturer | 1 | January 2, 2025 | 0 | 0 | 0 | api.fda.gov |
| Jiangsu Vedkang Medical Science and Technology Co.,Ltd. | Changzhou Jiangsu, China | Manufacturer | 1 | March 28, 2023 | 0 | 0 | 0 | api.fda.gov |
| Ningbo Xinwell Medical Technology Co., Ltd. | Cixi Zhejiang, China | Manufacturer | 1 | June 7, 2024 | 0 | 0 | 0 | api.fda.gov |
| Promisemed Hangzhou Meditech Co.,ltd. | Hangzhou Zhejiang, China | Exporter to the US, Manufacturer | 1 | July 12, 2024 | 0 | 0 | 0 | api.fda.gov |
| Yangzhou Fartley Medical Instrument Technology Co., Ltd | Yangzhou Jiangsu, China | Manufacturer | 1 | July 31, 2023 | 0 | 0 | 0 | api.fda.gov |
| Zhejiang Soudon Medical Technology Co.,ltd | Hangzhou Zhejiang, China | Manufacturer | 1 | January 26, 2024 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.