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Shenzhen Xinlianfeng Technology Co., Ltd

ChinaFDA applicant, unverified

Devices
1

What Shenzhen Xinlianfeng Technology Co., Ltd makes

Shenzhen Xinlianfeng Technology Co., Ltd manufactures electric nasal aspirators designed for infant and pediatric use, providing suction to clear nasal passages.

The company’s products are regulated as Class II devices under FDA 510(k) clearance requirements and are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Electric nasal aspirator Ref K222547

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Shenzhen Xinlianfeng Technology Co., Ltd have in the registry?

The registry currently lists 1 device for Shenzhen Xinlianfeng Technology Co., Ltd. Devices recorded under merged duplicate company entries are counted once.

Which registries list Shenzhen Xinlianfeng Technology Co., Ltd's devices?

Among its 1 most recently registered device, Shenzhen Xinlianfeng Technology Co., Ltd has devices listed in FDA 510(k) (1 device).

What risk classes do Shenzhen Xinlianfeng Technology Co., Ltd's devices fall under?

Among its 1 most recently registered device, the classes recorded for Shenzhen Xinlianfeng Technology Co., Ltd's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Shenzhen Xinlianfeng Technology Co., Ltd in the registry?

The most recently registered devices listed for Shenzhen Xinlianfeng Technology Co., Ltd include Electric nasal aspirator.

Generated automatically from registry data and not verified by a human reviewer.