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 Ceramed Corp. with 16 510(k) clearances. The most recent is a 510(k) clearance dated Aug 20, 1996: PERMARIDGE SYRINGE.
| Date | Record | Source |
|---|---|---|
| Aug 20, 1996 | PERMARIDGE SYRINGEK962838 · LYC | 510(k) clearances |
| Aug 1, 1996 | OSTEOGRAF STAINLESS STEEL SYRINGK962786 · LYC | 510(k) clearances |
| Apr 22, 1996 | OSTEOGRAF/N-300 HYDROXYLAPATITEK960348 · LYC | 510(k) clearances |
| Apr 18, 1996 | OSTEOGRAFT/N-700 HYDROXYLAPTITEK960368 · LYC | 510(k) clearances |
| Apr 18, 1996 | OSTEOGRAF/LD-300 HYDROXYLAPATITEK960353 · LYC | 510(k) clearances |
| Apr 15, 1996 | PERMAMESH-D HYDROXYLAPATITE MATRIXK960361 · LYC | 510(k) clearances |
| Mar 20, 1996 | PERMAMESH HYDROXYLAPATITE MATRIXK960362 · LZK | 510(k) clearances |
| Mar 20, 1996 | PERMAMESH-D HYDROXYLAPATITE MATRIXK960354 · LZK | 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
