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 Derata Corp. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Oct 31, 1988: DERATA MEDI-JECTOR V.
| Date | Record | Source |
|---|---|---|
| Oct 31, 1988 | DERATA MEDI-JECTOR VK883847 · KZE | 510(k) clearances |
| Feb 19, 1987 | DERATA MEDI-JECTOR IVK864561 · KZE | 510(k) clearances |
| Jul 5, 1985 | DERATA MEDI-JECTOR PROK844244 · KZE | 510(k) clearances |
| Nov 28, 1984 | DERATA MEDI-JECTOR IIIK844111 · KZE | 510(k) clearances |
| Mar 6, 1984 | MEDI-JECTOR IIK834044 · KZE | 510(k) clearances |
| Dec 8, 1977 | MEDI-JECTORK772129 · KZE | 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
