Skip to the page

Data / Medical devices / Reagents, Monkeypox Virus Nucleic Acid.

Reagents, Monkeypox Virus Nucleic Acid. (QTP): 6 FDA-registered makers in 1 country

6 establishments in 1 country are registered with the FDA to make Reagents, Monkeypox Virus Nucleic Acid. (product code QTP, Class N). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 0 510(k) clearances under this code, and lists 0 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
QTP
Device class
N
Medical specialty
Unknown

Makers by country

CountryMakers
United States6

Makers of Reagents, Monkeypox Virus Nucleic Acid.

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
Abbott Molecular, Inc.Des Plaines, IL, United StatesManufacturer0000api.fda.gov
CepheidSunnyvale, CA, United StatesManufacturer0000api.fda.gov
CepheidLodi, CA, United StatesManufacturer0000api.fda.gov
Roche Molecular Systems, Inc.Branchburg, NJ, United StatesManufacturer0000api.fda.gov
Roche Molecular Systems, Inc.Pleasanton, CA, United StatesSpecification developer0000api.fda.gov
Seegene Usa Inc.Irvine, CA, United StatesManufacturer0000api.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.