Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in NetherlandsLabelled 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 Polyganics B.V. with 9 510(k) clearances. The most recent is a 510(k) clearance dated Oct 23, 2014: HEMOPORE.
| Oct 23, 2014 | HEMOPOREK141816 · LYA | 510(k) clearances |
| Aug 7, 2014 | NASOPORE-FDK141423 · LYA | 510(k) clearances |
| Oct 20, 2011 | NEUROLAC(R) NERVE GUIDEK112267 · JXI | 510(k) clearances |
| May 7, 2007 | NASOPORE EARK070715 · NHB | 510(k) clearances |
| Oct 18, 2006 | NASOPORE EAR, MODELS ND04, ND05K062540 · KCN | 510(k) clearances |
| Nov 21, 2005 | NASOPORE NASAL DRESSING, MODEL NDOX-YYY/ZZK052099 · LYA | 510(k) clearances |
| May 4, 2005 | NEUROLAC NERVE GUIDEK050573 · JXI | 510(k) clearances |
| Nov 8, 2004 | VIVOSORB SHEET, MODEL FS01K042811 · FTL | 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
