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 London Intl., LLC with 6 510(k) clearances. The most recent is a 510(k) clearance dated Nov 16, 1998: DUREX LUBRAGEL LATEX CONDOM.
| Nov 16, 1998 | DUREX LUBRAGEL LATEX CONDOMK983380 · HIS | 510(k) clearances |
| Nov 16, 1998 | DUREX SENSIDOM LATEX CONDOMK982924 · HIS | 510(k) clearances |
| Aug 13, 1998 | DUREX COLORS AND SCENTSK980174 · HIS | 510(k) clearances |
| Jun 10, 1998 | STERILE, POWDERFREE LATEX EXAMINATION GLOVEK980785 · LYY | 510(k) clearances |
| May 20, 1998 | DUREX ULTRA COMFORTK980319 · HIS | 510(k) clearances |
| Apr 17, 1998 | DUREX LATEX CONDOMSK980204 · HIS | 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
