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Data / Medical devices / Test, Vaginal, Bacterial Sialidase

Test, Vaginal, Bacterial Sialidase (MXB): 3 FDA-registered makers in 2 countries

3 establishments in 2 countries are registered with the FDA to make Test, Vaginal, Bacterial Sialidase (product code MXB, Class 1, 21 CFR 866.2660). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 2 510(k) clearances under this code, the latest on April 6, 2005, and lists 1 recall event (0 Class I). FDA data exported November 2, 2026.

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Product code
MXB
Device class
1
Regulation
866.2660
Medical specialty
Microbiology

Makers by country

CountryMakers
United States2
Ireland1

Makers of Test, Vaginal, Bacterial Sialidase

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
Diagnostic Automation/ Cortez Diagnostics Inc,.Woodland Hills, CA, United StatesManufacturer0000api.fda.gov
Gryphus Diagnostics, L.L.C.Knoxville, TN, United StatesManufacturer0000api.fda.gov
Privapath Diagnostics LtdDublin 11 Dublin(County), IrelandManufacturer0000api.fda.gov

Updated April 6, 2005. 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.