Data / Medical devices / Nasopharyngoscope (Flexible Or Rigid) / China
FDA-registered makers of Nasopharyngoscope (Flexible Or Rigid) in China: 5 establishments
5 establishments in China are registered with the FDA to make Nasopharyngoscope (Flexible Or Rigid) (product code EOB). 4 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
- Nasopharyngoscope (Flexible Or Rigid)
- Product code
- EOB
- Country
- China
Makers of Nasopharyngoscope (Flexible Or Rigid) in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Hunan Vathin Medical Instrument Co., Ltd. | Xiangtan Hunan, China | Exporter to the US, Manufacturer | 2 | June 14, 2023 | 0 | 0 | 0 | api.fda.gov |
| Liaoning JRSD Commercial AND Trading Co.,Ltd. | Shenyang Liaoning, China | Manufacturer | 1 | August 25, 2017 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Hugemed Medical Technical Development Co., Ltd | Shenzhen Guangdong, China | Manufacturer | 1 | April 26, 2024 | 0 | 0 | 0 | api.fda.gov |
| Zhuhai Wesee Meditech Co., Ltd | Zhuhai Guangdong, China | Manufacturer | 1 | March 25, 2026 | 0 | 0 | 0 | api.fda.gov |
| Scivita Medical Technology Co., Ltd. | suzhou Jiangsu, China | 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.