Data / Medical devices / Container, Sharps / China
FDA-registered makers of Container, Sharps in China: 10 establishments
10 establishments in China are registered with the FDA to make Container, Sharps (product code MMK). 6 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Container, Sharps
- Product code
- MMK
- Country
- China
Makers of Container, Sharps in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Ningbo Maxcon Medical Technology Co., Ltd | Ningbo Zhejiang, China | Contract manufacturer, Exporter to the US, Manufacturer | 4 | June 16, 2023 | 0 | 0 | 0 | api.fda.gov |
| Zhejiang Gongdong Medical Technology Co., Ltd | TAIZHOU Zhejiang, China | Manufacturer | 3 | December 22, 2025 | 0 | 0 | 0 | api.fda.gov |
| Ningbo HSCC Medical Technology Co., Ltd | Ningbo Zhejiang, China | Manufacturer | 1 | September 2, 2010 | 0 | 0 | 0 | api.fda.gov |
| Promisemed Hangzhou Meditech Co.,ltd. | Hangzhou Zhejiang, China | Exporter to the US, Manufacturer | 1 | November 17, 2021 | 0 | 0 | 0 | api.fda.gov |
| Taizhou Huangyan Guanhong Plastic Steel Products Factory | Taizhou Zhejiang, China | Manufacturer | 1 | May 22, 2026 | 0 | 0 | 0 | api.fda.gov |
| Unisource Shanghai Ltd. | Shanghai, China | Exporter to the US, Repackager or relabeler, Reprocessor | 1 | January 25, 2007 | 0 | 0 | 0 | api.fda.gov |
| Dongguan Yee Hing Foon Plastic Co., Ltd. / Hope Come International | Dongguan City Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Gcmedica Enterprise Ltd. (wuxi) | Wuxi Jiangsu, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Gcmedica Enterprise Ltd.(wuxi) | WUXI Jiangsu, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jie Gao Plastic Products Co., Ltd. | DONGGUAN CITY Guangdong, 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.