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Data / Medical devices / Sperm, Antigen, Antiserum, Control

Sperm, Antigen, Antiserum, Control (DFQ): 9 FDA-registered makers in 4 countries

9 establishments in 4 countries are registered with the FDA to make Sperm, Antigen, Antiserum, Control (product code DFQ, Class 1, 21 CFR 866.5800). 0 of them have a 510(k) clearance or PMA approval on file and 1 has a recall event. The FDA has issued 0 510(k) clearances under this code, and lists 2 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
DFQ
Device class
1
Regulation
866.5800
Medical specialty
Immunology

Makers by country

CountryMakers
China6
United States1
Germany1
Belgium1

Makers of Sperm, Antigen, Antiserum, Control

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Assure Tech. (hangzhou) Co., Ltd.Hangzhou Zhejiang, ChinaComplaint file establishment, Manufacturer0000api.fda.gov
Assure Tech. (Hangzhou) Co., Ltd.Hangzhou Zhejiang, ChinaManufacturer0000api.fda.gov
Bioteke Corporation (wuxi) Co., LtdWuxi City Jiangsu, ChinaManufacturer0000api.fda.gov
Changchun Merydi Bio-Tech Co., Ltd.changchun Jilin, ChinaManufacturer0000api.fda.gov
Changchun Wancheng Bio-Electron Co., Ltd.Changchun Jilin, ChinaManufacturer0010api.fda.gov
CalibreScientific US, Inc.Vancouver, WA, United StatesManufacturer0000api.fda.gov
DRG Instruments GMBHMARBURG Hesse, GermanyComplaint file establishment, Manufacturer0000api.fda.gov
DiaSource ImmunoAssays, SALouvain-La-Neuve Brabant Wallon, BelgiumManufacturer0000api.fda.gov
Jilin Hongyi Bio-Tech Co., Ltd.Changchun Jilin, ChinaExporter to the US, Manufacturer0000api.fda.gov

Updated November 2, 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.