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 Biomedia with 19 510(k) clearances. The most recent is a 510(k) clearance dated Jun 2, 1982: #2010 CAMPHYLOBACTER AGAR.
| Date | Record | Source |
|---|---|---|
| Jun 2, 1982 | #2010 CAMPHYLOBACTER AGARK821300 · JSI | 510(k) clearances |
| Jun 1, 1982 | #50002 QUAD DIAGNOSTIC SYSTEMK821301 · JSI | 510(k) clearances |
| Jun 1, 1982 | #50003 QUAD DIAGNOSTIC SYSTEMK821302 · JSH | 510(k) clearances |
| May 13, 1982 | BI PLATE-XLD/HEKTOEN #30012K821108 · JSI | 510(k) clearances |
| Jun 18, 1981 | TRYPTIC SOY AGAR W/5% SHEEP BLOOD & EMBK811474 · JSI | 510(k) clearances |
| Jun 18, 1981 | EMB AGAR, LEVINEK811478 · JSI | 510(k) clearances |
| Jun 18, 1981 | THAYER MARTIN AGARK811476 · JTY | 510(k) clearances |
| Jun 18, 1981 | TRYPTIC SOY AGAR W/5% & 10% SHEEP BLOODK811475 · JSG | 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
