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Data / Medical devices / Reagent, Rickettsia Serological / United States

FDA-registered makers of Reagent, Rickettsia Serological in the United States: 7 establishments

7 establishments in the United States are registered with the FDA to make Reagent, Rickettsia Serological (product code LSQ). 1 has a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device
Reagent, Rickettsia Serological
Product code
LSQ
Country
United States

Makers of Reagent, Rickettsia Serological in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
GenbioSan Diego, CA, United StatesManufacturer2March 13, 1998000api.fda.gov
DiaSorin Molecular LLCCypress, CA, United StatesManufacturer0000api.fda.gov
Immucor, Inc.Norcross, GA, United StatesManufacturer0000api.fda.gov
Inbios International, Inc.Seattle, WA, United StatesManufacturer for export0000api.fda.gov
STS CorporationDuluth, GA, United StatesComplaint file establishment, Repackager or relabeler, Specification developer0000api.fda.gov
VMRD, Inc.Fullerton, CA, United StatesManufacturer0000api.fda.gov
Zeus Scientific LLCBranchburg, NJ, 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.