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Data / Medical devices / China / Yian Medical Technology (haining) Co., Ltd.

Yian Medical Technology (haining) Co., Ltd.: FDA-registered device maker in Jiaxing City, Zhejiang, China, 2 510(k) clearances

Yian Medical Technology (haining) Co., Ltd. is registered with the FDA (registration 3023322470) in Jiaxing City, Zhejiang, China. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated June 27, 2025. 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
3023322470
Address
1st Floor Area 1,2nd Floor Area 1,Building A, No. 2 Caohejing Road, Haining Economic Development Zone, Haichang Street, Haining City, Jiaxing City, Zhejiang, China, 314400
Owner or operator
Yian Medical Technology (Haining) Co., Ltd. (10085179)
Roles
Manufacturer, Specification developer
First device listed
January 11, 2024
Registered through
2026
Brand names listed
Dental CBCT X-ray System, OAS - X-ray, tomography, computed, dental

Devices it lists

DeviceProduct codeClassRoleSource
X-Ray, Tomography, Computed, DentalOAS2Manufacturer, 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
June 27, 2025K251642Dental CBCT X-ray SystemOASSubstantially EquivalentYian Medical Technology (Haining) Co., Ltd.accessdata.fda.gov
January 9, 2024K232710Dental Cone-beam Computed TomographyOASSubstantially EquivalentYian Medical Technology (Haining) Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated June 27, 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.