Diagnostics makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 10 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Bio-Rad Laboratories and its 6 subsidiaries with 620 510(k) clearances, 28 device recalls and 1 AI-enabled device. The most recent is a device recall dated Apr 3, 2019: Autoimmune EIA Anti-Tissue Transglutaminase (tTG) IgA Test; Material Number 425-2260; Lo….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Bio-Rad Laboratories and its 6 subsidiaries
A hatched bar is a year that is not over, so its count covers only part of the year.
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
