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 13, 2026, FDA's public records list Eagle Twe, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Aug 19, 2005: DIVAS DUAL PLEASURE MALE LATEX CONDOM.
| Aug 19, 2005 | DIVAS DUAL PLEASURE MALE LATEX CONDOMK051273 · HIS | 510(k) clearances |
| Mar 30, 2001 | SHEER THIN AROMAS RED LATEX CONDOMK010028 · HIS | 510(k) clearances |
| Mar 29, 2001 | SHEER THIN AROMAS YELLOW LATEX CONDOMK004051 · HIS | 510(k) clearances |
| Mar 27, 2001 | SHEER THIN AROMAS GREEN LATEX CONDOMK004036 · HIS | 510(k) clearances |
| Mar 27, 2001 | SHEER THIN AROMAS BLUE LATEX CONDOMK004016 · 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
