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Data / Medical devices / Test, Immunity, Cell Mediated, Mycobacterium Tuberculosis

Test, Immunity, Cell Mediated, Mycobacterium Tuberculosis (NCD): 4 FDA-registered makers in 2 countries

4 establishments in 2 countries are registered with the FDA to make Test, Immunity, Cell Mediated, Mycobacterium Tuberculosis (product code NCD, Class 3). 2 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.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Product code
NCD
Device class
3
Medical specialty
Unknown

Makers by country

CountryMakers
United States3
Italy1

Makers of Test, Immunity, Cell Mediated, Mycobacterium Tuberculosis

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
DiaSorin Italia S.p.A.SALUGGIA Vercelli, ItalyManufacturer0100api.fda.gov
QiagenGermantown, MD, United StatesManufacturer0110api.fda.gov
Diasorin Inc.Stillwater, MN, United StatesContract manufacturer0000api.fda.gov
Diagnostic Automation/ Cortez Diagnostics Inc,.Woodland Hills, CA, United StatesManufacturer, Repackager or relabeler0000api.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.