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 Ceremed with 20 510(k) clearances. The most recent is a 510(k) clearance dated Sep 27, 2016: Biopor Porous Polyethylene Implants.
| Sep 27, 2016 | Biopor Porous Polyethylene ImplantsK161446 · GWO | 510(k) clearances |
| Jul 14, 2016 | Biopor, AOC Porous Polyethylene, CereporK160988 · KKY | 510(k) clearances |
| Apr 16, 2015 | BIOPOR AOC POROUS POLYETHYLENE, CEREPORK141880 · KKY | 510(k) clearances |
| Sep 12, 2013 | ADAPTAIN, ADAPTAIN FASTWRAP, ENVELOCK, BIOWAIK132198 · KHJ | 510(k) clearances |
| Nov 27, 2012 | ADAPTAIN FASTWRAP, ENVELOCK, GRAFTAINK122561 · KHJ | 510(k) clearances |
| Jun 6, 2012 | ADAPTAIN SOLUBLE IMPLANT MATERIALK120220 · KHJ | 510(k) clearances |
| Jan 5, 2011 | CERETENE SOLUBLE IMPLANT MATERIALK103047 · KHJ | 510(k) clearances |
| Oct 8, 2010 | OSTENE CT, AOC CT, OSTEOTENE, CERETENEK102071 · MTJ | 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
