Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Brilliant Ray International with 7 510(k) clearances. The most recent is a 510(k) clearance dated May 25, 1989: PATIENT EXAM GLOVES (MFG. YU HUA LATEX FACTORY).
| May 25, 1989 | PATIENT EXAM GLOVES (MFG. YU HUA LATEX FACTORY)K892022 · LYY | 510(k) clearances |
| May 25, 1989 | PATIENT EXAM GLOVES (MFG. BEIJING LATEX FACTORY)K892025 · LYY | 510(k) clearances |
| May 25, 1989 | PATIENT EXAM GLOVES (MFG. XIAN WELFARE LATEX )K892023 · LYY | 510(k) clearances |
| May 25, 1989 | PATIENT EXAM GLOVES (MFG. CHAGAN TANG CAPITOL)K892024 · LYY | 510(k) clearances |
| May 4, 1989 | PATIENT EXAMINATION GLOVES (LATEX)K892109 · LYY | 510(k) clearances |
| Apr 14, 1989 | PATIENT EXAM GLOVE (LATEX) MFG. TIANJIN JI COUNTYK891739 · LYY | 510(k) clearances |
| Apr 14, 1989 | PATIENT EXAM GLOVES (LATEX) MFG. TIANJIN KANG BAOK891740 · 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
