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Data / Medical devices / Kit, First Aid, Talking / China

FDA-registered makers of Kit, First Aid, Talking in China: 14 establishments

14 establishments in China are registered with the FDA to make Kit, First Aid, Talking (product code OVR). 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
Kit, First Aid, Talking
Product code
OVR
Country
China

Makers of Kit, First Aid, Talking in China

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Amis (xiamen) Cultural Creativity Co., LtdXiamen Fujian, ChinaManufacturer0000api.fda.gov
Chants (foshan) Technology Co.,ltdFoshan Guangdong, ChinaExporter to the US, Manufacturer, Repackager or relabeler0000api.fda.gov
Hangzhou Rollmed Co.,ltd.Hangzhou Zhejiang, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Hynaut Health Technology Co., LTD.Qingdao Shandong, ChinaManufacturer0000api.fda.gov
Jiangsu Saikang Medical Equipment Co., LtdZhangjiagang Jiangsu, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Jiangsu Taimedical Technology Co., LtdNanjing Jiangsu, ChinaExporter to the US, Manufacturer0000api.fda.gov
Jiangsu Yongfa Medical Equipment Technology Co., LtdZhangjiagang City Jiangsu, ChinaManufacturer0000api.fda.gov
Jiangsu Hongsheng Bioengineering Co., Ltd.Nantong Jiangsu, ChinaExporter to the US, Manufacturer0000api.fda.gov
Shanghai No. 2 Medical College Duhang Medical Equipment FactoryShanghai, ChinaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Shenyang Ourpromise Medical Equipment Co., Ltd.Shenyang Liaoning, ChinaExporter to the US, Manufacturer0000api.fda.gov
Wenzhou Caretek Medical Device Co., LtdWenzhou Zhejiang, ChinaContract manufacturer0000api.fda.gov
Wenzhou Longwan Medical Device FactoryWenzhou Zhejiang, ChinaManufacturer0000api.fda.gov
Yadu Medical (henan) Co., LtdChangyuan Henan, ChinaManufacturer0000api.fda.gov
Yiwu Ori-Power Medtech Co., Ltd.YIWU Zhejiang, ChinaExporter to the US, Manufacturer0000api.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.