Data / Medical devices / Camera, Ophthalmic, General-Use / China
FDA-registered makers of Camera, Ophthalmic, General-Use in China: 12 establishments
12 establishments in China are registered with the FDA to make Camera, Ophthalmic, General-Use (product code PJZ). 0 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
- Camera, Ophthalmic, General-Use
- Product code
- PJZ
- Country
- China
Makers of Camera, Ophthalmic, General-Use in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Chongqing Bio Newvision Medical Equipment Ltd. | Chongqing, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Chongqing Kanghua Ruiming S&T Co., Ltd. | Chongqing, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Chongqing SS Medical Equipments Co., Ltd | Chongqing, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Chongqing Sunkingdom Medical Instrument Co.,ltd | Chongqing, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Changsha Airdoc Health Technology Co., Ltd. | Changsha Hunan, China | Contract manufacturer, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hangzhou Ai-Mu Meditec Co., Ltd. | Hangzhou Zhejiang, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Main Meditech Co., Ltd | Chongqing, China | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ningbo Ming Sing Optical R&D Co., Ltd. | Ningbo Zhejiang, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shanghai Link Instruments Co.,ltd | Changzhou City Jiangsu, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shanghai Mediworks Precision Instruments Co., Ltd. | Shanghai, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shenzhen Create Technology Co.,ltd | Shenzhen Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Visuscience Meditech Co., Ltd. | WUXI 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.