Skip to the page

Data / Medical devices / Enzyme Linked Immunoabsorbent Assay, Rubeola Igg / United States

FDA-registered makers of Enzyme Linked Immunoabsorbent Assay, Rubeola Igg in the United States: 6 establishments

6 establishments in the United States are registered with the FDA to make Enzyme Linked Immunoabsorbent Assay, Rubeola Igg (product code LJB). 2 have a 510(k) clearance or PMA approval on file and 2 have a recall event. 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.

Device
Enzyme Linked Immunoabsorbent Assay, Rubeola Igg
Product code
LJB
Country
United States

Makers of Enzyme Linked Immunoabsorbent Assay, Rubeola Igg in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Gold Standard Diagnostics, LLCDavis, CA, United StatesRepackager or relabeler, Specification developer1January 28, 1998000api.fda.gov
Trinity Biotech USAJamestown, NY, United StatesManufacturer1February 24, 1988000api.fda.gov
Bio-Rad Laboratories, Inc.Woodinville, WA, United StatesContract manufacturer, Specification developer0000api.fda.gov
Bio-Rad Laboratories, Inc.Hercules, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Calbiotech, Inc.El Cajon, CA, United StatesContract manufacturer0010api.fda.gov
Zeus Scientific LLCBranchburg, NJ, United StatesManufacturer0010api.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.