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 14, 2026, FDA's public records list Trylon Corp. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Nov 22, 2004: VIZILITE-BLUE ORAL EXAM KIT.
| Nov 22, 2004 | VIZILITE-BLUE ORAL EXAM KITK033033 · EAZ | 510(k) clearances |
| Feb 22, 2002 | SPIRABRUSH CX BIOPSY INSTRUMENTK011488 · HFB | 510(k) clearances |
| Nov 27, 2001 | ORALLITE COMPREHENSIVE EXAM TRAYK012070 · MPU | 510(k) clearances |
| Mar 16, 2001 | SPECULITE/ORALLITEK003995 · EAZ | 510(k) clearances |
| Dec 12, 1997 | SPECULITEK963391 · MPU | 510(k) clearances |
| Mar 21, 1996 | PAP PLUS SPECULOSCOPY COMPREHENSIVE PELVIC EXAM TRAYK955790 · HIC | 510(k) clearances |
| Dec 8, 1995 | SPECULITEK953364 · HET | 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
