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Data / Medical devices / China / Allgens Medical Technology Co.,Ltd.

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

Allgens Medical Technology Co.,Ltd. is registered with the FDA (registration 3012270469) in Beijing, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated July 9, 2015. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3012270469
Address
1st floor and Rooms,,2nd Building,No.26 Yongwang west road,Daxing district, Beijing, China, 102609
Owner or operator
Allgens Medical Technology Co.,Ltd (10050079)
Roles
Complaint file establishment, Manufacturer
First device listed
October 10, 2015
Registered through
2026
Brand names listed
Bongold

Devices it lists

DeviceProduct codeClassRoleSource
Filler, Bone Void, Calcium CompoundMQV2Complaint file establishment, 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
July 9, 2015K141725BONGOLD BONE GRAFT MATERIALMQVSubstantially EquivalentBeijing Allgens Medical Science & Technology Co, Laccessdata.fda.gov

Compare with other makers

Updated July 9, 2015. 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.