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Data / Medical devices / China / Ningbo Ranor Medical Science & Technology Co., Ltd.

Ningbo Ranor Medical Science & Technology Co., Ltd.: FDA-registered device maker in Ningbo Zhejiang, China, 5 510(k) clearances

Ningbo Ranor Medical Science & Technology Co., Ltd. is registered with the FDA (registration 3016719957) in Ningbo Zhejiang, China. It lists 7 device types. The FDA files 5 510(k) clearances under its listings, the newest dated January 9, 2026. Registered through 2026. FDA data exported November 3, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
3016719957
Address
No. 127 Fenghui Road, Wangchun Industrial Park Haishu District, Ningbo Zhejiang, China, 315171
Owner or operator
Ningbo Ranor Medical Science & Technology Co., Ltd. (10075629)
Roles
Contract manufacturer, Foreign private label distributor, Manufacturer
First device listed
June 21, 2020
Registered through
2026
Brand names listed
Arm Blood Pressure Monitor, Arm Blood Pressure Monitor (MJ1D,MJ1DS,MJ3D,MJ5D,MJ6D,MJ8D,RN3D,MJ4D,RN1D,RN2D), Arm Blood Pressure Monitor (Model MJ1L, MJ2L, RN3L, RN4L, RN5L), Dental Scaler; RN1Y, Dental Scaler; RN2Y, Dental Scaler; RN3Y, Dental Scaler; RN4Y, Dental Scaler; RN5Y and more

Devices it lists

DeviceProduct codeClassRoleSource
Continuous Measurement ThermometerFLL2Manufactureraccessdata.fda.gov
Dilator, NasalLWF1Contract manufacturer, Foreign private label distributoraccessdata.fda.gov
Pack, Hot Or Cold, DisposableIMD1Contract manufacturer, Foreign private label distributoraccessdata.fda.gov
Scaler, PeriodonticEMN1Manufactureraccessdata.fda.gov
Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)HOY1Contract manufacturer, Foreign private label distributoraccessdata.fda.gov
System, Measurement, Blood-Pressure, Non-InvasiveDXN2Manufactureraccessdata.fda.gov
Tape And Bandage, AdhesiveKGX1Contract manufacturer, Foreign private label distributoraccessdata.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
January 9, 2026K253142Arm Blood Pressure Monitor (MJ1D,MJ1DS,MJ3D,MJ5D,MJ6D,MJ8D,RN3D,MJ4D,RN1D,RN2D)DXNSubstantially EquivalentNingbo Ranor Medical Technology Co., Ltd.accessdata.fda.gov
December 19, 2025K251143Arm Blood Pressure Monitor (MJ1L, MJ2L, RN3L, RN4L,RN5L)DXNSubstantially EquivalentNingbo Ranor Medical Science & Technology Co., Ltd.accessdata.fda.gov
July 16, 2020K200578Infrared Thermometer Model Number RN-50A,RN-50BFLLSubstantially EquivalentNingbo Ranor Medical Science & Technology Co., Ltd.accessdata.fda.gov
July 16, 2020K193456Arm Blood Pressure MonitorDXNSubstantially EquivalentNingbo Ranor Medical Science & Technology Co., Ltd.accessdata.fda.gov
June 19, 2020K200471Infrared Thermometer Model Number RN-60A,RN-60BFLLSubstantially EquivalentNingbo Ranor Medical Science & Technology Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated January 9, 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.