Data / Medical devices / Gauze/Sponge, Internal / China
FDA-registered makers of Gauze/Sponge, Internal in China: 6 establishments
6 establishments in China are registered with the FDA to make Gauze/Sponge, Internal (product code EFQ). 1 has 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
- Gauze/Sponge, Internal
- Product code
- EFQ
- Country
- China
Makers of Gauze/Sponge, Internal in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Derma Sciences Nantong Incorporation | DEVELOPMENT Jiangsu, China | Contract manufacturer, Manufacturer | 2 | April 29, 1998 | 0 | 0 | 0 | api.fda.gov |
| Allmed Medical Products Co., Ltd. | Zhijiang City Hubei, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Allmed Medical Products Co., Ltd. | ZHIJIANG CITY Hubei, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Anqing Aijing Textile Co., Ltd. | AnQing City Anhui, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jianerkang Medical Co., Ltd. | Changzhou City Jiangsu, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Suzhou Avon Textile Co., Ltd. | Suzhou City Jiangsu, 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.