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 Anatech, Ltd. with 14 510(k) clearances. The most recent is a 510(k) clearance dated Jul 28, 1988: ZINC FORMALIN.
| Jul 28, 1988 | ZINC FORMALINK882874 · LDX | 510(k) clearances |
| Jul 28, 1988 | FIELDTEX HEMATOXYLINK882873 · KQC | 510(k) clearances |
| Jun 15, 1988 | ZINC FORMALIN CONCENTRATEK882268 · IGG | 510(k) clearances |
| Apr 5, 1988 | XYLENEK881282 · KEM | 510(k) clearances |
| Aug 6, 1987 | DRY-FORMK872663 · IFP | 510(k) clearances |
| Jul 9, 1987 | ANATECH HEMATOXYLIN-NORMAL STRENGTHK872499 · HYJ | 510(k) clearances |
| Jul 9, 1987 | HARRIS HEMATOXYLINK872498 · HYK | 510(k) clearances |
| Jul 9, 1987 | ANATECH HEMATOXYLIN-EXTRA STRENGTHK872500 · HYJ | 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
