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Data / Medical devices / China / Xiamen Taotao Technology Co., Ltd.

Xiamen Taotao Technology Co., Ltd.: FDA-registered device maker in Xiamen City Fujian, China, 1 510(k) clearance

Xiamen Taotao Technology Co., Ltd. is registered with the FDA (registration 3027619563) in Xiamen City Fujian, China. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 23, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3027619563
Address
2F, No. 23, 260 Huanzhu Road, Jimei District, Xiamen City Fujian, China, 361000
Owner or operator
Xiamen Taotao Technology Co., Ltd. (10088317)
Roles
Manufacturer, Specification developer
First device listed
June 28, 2023
Registered through
2026
Brand names listed
Alternating Air Pressure Mattress and Pump(Models: MA101BL,MA102BL,MA101BK,MA102BK), Alternating Pressure Mattress System(model: AAPS-TT-0301,AAPS-TT-0301S), Alternating Pressure Mattress System(model: AAPS-TT-0301SQ), Alternating pressure mattress, Alternating pressure mattress(model: TT-APM-01), Alternating pressure mattress(model: TT-APM-02), Alternating pressure mattress(model: TT-APM-03), Alternating pressure mattress(model: TT-APM-04) and more

Devices it lists

DeviceProduct codeClassRoleSource
Cushion, FlotationKIC1Manufacturer, Specification developeraccessdata.fda.gov
Massager, Powered Inflatable TubeIRP2Manufacturer, Specification developeraccessdata.fda.gov
Mattress, Air Flotation, Alternating PressureFNM2Manufacturer, Specification developeraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
July 23, 2025K242615Intermittent pressure compression system (Compression Pump PT1005A; Leg Compression Cuffs; L-1001S, L-1001L, L-1001XL, L-1001XXL, L-1001XXXL)IRPSubstantially EquivalentXiamen Taotao Technology Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated July 23, 2025. 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.