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Data / Medical devices / China / Shenzhen Ruiankang Technology Co., Ltd.

Shenzhen Ruiankang Technology Co., Ltd.: FDA-registered device maker in Shenzhen Guangdong, China, 1 510(k) clearance

Shenzhen Ruiankang Technology Co., Ltd. is registered with the FDA (registration 3016707048) in Shenzhen Guangdong, China. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 10, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3016707048
Address
Floor 1 and 2, No. 8, Zhugushi Chunyang Industrial Park, Wulian Community, Longgang Street, Longgang District, Shenzhen Guangdong, China, 518100
Owner or operator
Shenzhen Ruiankang Technology Co., Ltd. (10090962)
Roles
Manufacturer
First device listed
February 28, 2025
Registered through
2026
Brand names listed
Blood Pressure Monitor (RAK260, RAK262, RAK263, RAK266, RAK268, RAK269), Blood Pressure Monitor (RAK282, RAK283, RAK286, RAK288, RAK289), Blood Pressure Monitor (RAK291, RAK292, RAK293, RAK295, RAK296, RAK297, RAK298), Blood Pressure Monitor, models P116, P126, P136, SK10, P608, RAK288A, RAK289A, RAK289B, P288, Blood Pressure Monitor, models RAK260L, RAK261L, RAK262L, RAK263L, RAK266L, RAK268L, RAK269L, Blood Pressure Monitor, models RAK261, RAK281, RAK285, RAK290, RAK299, Blood Pressure Monitor, models RAK268T, RAK283T, RAK288T, RAK289T, P100, RAK288G, RAK289G, P108, Blood Pressure Monitor, models RAK280L, RAK281L, RAK282L, RAK283L, RAK285L, RAK286L, RAK288L, RAK289L and more

Devices it lists

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
January 10, 2025K242528Blood Pressure Monitor (RAK260, RAK262, RAK263, RAK266, RAK268, RAK269, RAK282, RAK283, RAK286, RAK288, RAK289, RAK291, RAK292, RAK293, RAK295, RAK296, RAK297, RAK298)DXNSubstantially EquivalentShenzhen Ruiankang Technology Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated January 10, 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.