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 15, 2026, FDA's public records list R. Kent Richards, Inc. with 12 510(k) clearances. The most recent is a 510(k) clearance dated Apr 14, 1987: CHLAMYDIA & VIRAL TRANSPORT MEDIUM.
| Apr 14, 1987 | CHLAMYDIA & VIRAL TRANSPORT MEDIUMK871065 · JSM | 510(k) clearances |
| Nov 18, 1985 | MANNITOL SALT AGARK854452 · JSI | 510(k) clearances |
| Nov 18, 1985 | CDC ANAEROBE BLOOD AGARK854455 · JSG | 510(k) clearances |
| Nov 18, 1985 | COLUMBIA CNA AGAR W/5% SHEEP BLOODK854457 · JSJ | 510(k) clearances |
| Nov 18, 1985 | TRYPTIC SOY BLOOD AGARK854454 · KZI | 510(k) clearances |
| Nov 18, 1985 | HEKTOEN ENTERIC AGARK854449 · JSI | 510(k) clearances |
| Nov 18, 1985 | BILE ESCULIN AZIDE AGARK854450 · JSI | 510(k) clearances |
| Nov 18, 1985 | P.E.Z. AGAR (PHENYLETHANOL AGAR)K854453 · JSJ | 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
