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Data / Medical devices / Antigens, Ha, Treponema Pallidum

Antigens, Ha, Treponema Pallidum (GMT): 3 FDA-registered makers in 3 countries

3 establishments in 3 countries are registered with the FDA to make Antigens, Ha, Treponema Pallidum (product code GMT, Class 2, 21 CFR 866.3830). 2 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 9 510(k) clearances under this code, the latest on November 13, 1997, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
GMT
Device class
2
Regulation
866.3830
Medical specialty
Microbiology

Makers by country

CountryMakers
United States1
Japan1
China1

Makers of Antigens, Ha, Treponema Pallidum

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
Fujirebio Diagnostics, Inc.Seguin, TX, United StatesManufacturer1November 13, 1997000api.fda.gov
Fujirebio Inc. Ube FacilityYamaguchi, JapanManufacturer1November 13, 1997000api.fda.gov
Zhuhai Livzon Diagnostics Inc.Zhuhai Guangdong, ChinaContract manufacturer0000api.fda.gov

Updated November 13, 1997. 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.