Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 4 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list SSL Americas with 17 510(k) clearances. The most recent is a 510(k) clearance dated Jun 19, 2008: DUREX SYNTHETIC POLYISOPRENE MALE CONDOM.
| Jun 19, 2008 | DUREX SYNTHETIC POLYISOPRENE MALE CONDOMK072169 · MOL | 510(k) clearances |
| May 7, 2008 | DUREX PLAY TINGLING AQUEOUS BASED LUBRICANTK072236 · NUC | 510(k) clearances |
| Apr 1, 2008 | DUREX PLAY SOFT & SENSUAL LUBRICANTK071626 · NUC | 510(k) clearances |
| Mar 10, 2008 | DUREX PLAY MASSAGE GEL LUBRICANTK063385 · NUC | 510(k) clearances |
| Jun 8, 2006 | DUREX PLAY TEMPTATIONS ASSORTED LUBRICANTSK060098 · NUC | 510(k) clearances |
| Jan 27, 2006 | DUREX MALE COLORED LATEX CONDOMS WITH SCENTED LUBRICANTSK052959 · HIS | 510(k) clearances |
| Apr 8, 2005 | DUREX PLAY TINGLING LUBRICANTK042958 · NUC | 510(k) clearances |
| Apr 5, 2005 | DUREX SPEARMINT SCENTED LUBRICATED LATEX CONDOM (DUREX 'TINGLING PLEASURE' CONDOMK042470 · 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
