FirmLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA files no records under this name; these are its 2 companies' records, each linked to the record.
As of Nov 14, 2026, FDA's public records list Schneider Electric and its 2 subsidiaries with 1 drug application and 1 510(k) clearance. The most recent is a 510(k) clearance dated Jul 14, 1989: PATIENT EXAMINATION GLOVES (LATEX).
| Date | Record | Source |
|---|---|---|
| Jul 14, 1989 | PATIENT EXAMINATION GLOVES (LATEX)K892703 ยท LYY | 510(k) clearances |
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
