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Data / Medical devices / China / Jiangsu Rayer Medical Technology Co., Ltd.

Jiangsu Rayer Medical Technology Co., Ltd.: FDA-registered device maker in Wuxi Jiangsu, China, 1 510(k) clearance

Jiangsu Rayer Medical Technology Co., Ltd. is registered with the FDA (registration 3014113695) in Wuxi Jiangsu, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated May 1, 2020. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3014113695
Address
No.99 Furongzhongsan Road, Xishan Economic Development Zone, 214192 Wuxi, Wuxi Jiangsu, China, 214192
Owner or operator
Jiangsu Rayer Medical Technology Co., Ltd. (10075833)
Roles
Manufacturer
First device listed
June 28, 2020
Registered through
2026
Brand names listed
Image Guidance System for Radiotherapy

Devices it lists

DeviceProduct codeClassRoleSource
Accelerator, Linear, MedicalIYE2Manufactureraccessdata.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
May 1, 2020K192405Image Guidance System for RadiotherapyIYESubstantially EquivalentJiangsu Rayer Medical Technology Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated May 1, 2020. 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.