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Data / Medical devices / China / Anhui Miisen Intelligence Technology Co., Ltd.

Anhui Miisen Intelligence Technology Co., Ltd.: FDA-registered device maker in Wuhu Anhui, China, 1 510(k) clearance

Anhui Miisen Intelligence Technology Co., Ltd. is registered with the FDA (registration 3031915955) in Wuhu Anhui, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated May 31, 2024. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3031915955
Address
B6, Zone B, Chungu 3D Printing Intelligent Equipment Industrial Park Fanchang Economic Development Zone, Wuhu Anhui, China, 241200
Owner or operator
Anhui Miisen Intelligence Technology Co., Ltd. (10091251)
Roles
Exporter to the US, Manufacturer
First device listed
August 1, 2024
Registered through
2026
Brand names listed
Dental Zirconia Block (Models HT-plus, ST, SHT, UT, 3D-Pro)

Devices it lists

DeviceProduct codeClassRoleSource
Powder, PorcelainEIH2Exporter to the US, Manufactureraccessdata.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 31, 2024K240912Dental Zirconia Block (Models HT-plus, ST, SHT, UT, 3D-Pro)EIHSubstantially EquivalentAnhui Miisen Intelligence Technology Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated May 31, 2024. 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.