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Xiamen Taotao Technology Co., Ltd.

ChinaFDA applicant, unverified FDA FEI 3027619563

Devices
1
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

What Xiamen Taotao Technology Co., Ltd. makes

The company manufactures intermittent pressure compression systems, including motorised pumps and customisable leg compression cuffs designed for venous circulation support. The portfolio includes adjustable-length cuffs (sizes L-1001S through L-1001XXXL) and a dedicated compression pump (PT1005A) for sequential pressure therapy.

These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company operates from 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

Company details

FDA FEI number
3027619563
Address
2F, No. 23, 260 Huanzhu Road, Jimei District, Xiamen City Fujian

Frequently asked questions

How many devices does Xiamen Taotao Technology Co., Ltd. have in the registry?

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

Which registries list Xiamen Taotao Technology Co., Ltd.'s devices?

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

What risk classes do Xiamen Taotao Technology Co., Ltd.'s devices fall under?

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

What are the newest devices from Xiamen Taotao Technology Co., Ltd. in the registry?

The most recently registered devices listed for Xiamen Taotao Technology Co., Ltd. include Intermittent pressure compression system (Compression Pump PT1005A; Leg Compression Cuffs; L-1001S, L-1001L, L-1001XL, L-1001XXL, L-1001XXXL).

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