Data / Medical devices / Case, Contact Lens / China
FDA-registered makers of Case, Contact Lens in China: 5 establishments
5 establishments in China are registered with the FDA to make Case, Contact Lens (product code LRX). 5 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
- Case, Contact Lens
- Product code
- LRX
- Country
- China
Makers of Case, Contact Lens in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Danyang Chanxin Glasses Cases Factory | Danyang Jiangsu, China | Exporter to the US, Manufacturer | 1 | June 7, 2016 | 0 | 0 | 0 | api.fda.gov |
| Ningbo Kaida Rubber And Plastic Technology Co., Ltd | Yu Yao City, Zhejiang Province, China | Manufacturer | 1 | May 1, 2007 | 0 | 0 | 0 | api.fda.gov |
| Ningbo Haishu Zonghai Artware Co., Ltd. | Ningbo City Zhejiang, China | Manufacturer | 1 | December 9, 2016 | 0 | 0 | 0 | api.fda.gov |
| Shun Sze Industrial (shenzhen) Co., Ltd | SHENZHEN Guangdong, China | Contract manufacturer, Manufacturer | 1 | November 30, 2017 | 0 | 0 | 0 | api.fda.gov |
| Shanghai Care Us Medical Product Co., Ltd. | Shanghai, China | Exporter to the US, Manufacturer | 1 | October 9, 2024 | 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.