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 Biohytech International, Inc. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Mar 24, 1987: DS-DNA EIA DIAGNOSTIC KIT.
| Mar 24, 1987 | DS-DNA EIA DIAGNOSTIC KITK870453 · LJM | 510(k) clearances |
| Mar 17, 1987 | SM EIA DIAGNOSTIC KITK870455 · LJM | 510(k) clearances |
| Mar 17, 1987 | DNP EIA DIAGNOSTIC KITK870456 · LJM | 510(k) clearances |
| Mar 17, 1987 | HISTONES EIA DIAGNOSTIC KITK870458 · DHN | 510(k) clearances |
| Mar 17, 1987 | RNP EIA DIAGNOSTIC KITK870457 · LJM | 510(k) clearances |
| Mar 17, 1987 | SS-DNA EIA DIAGNOSTIC KITK870452 · LJM | 510(k) clearances |
| Oct 24, 1986 | ANA-ENZYME IMMUNOASSAY (ANA-EIA) DIAGNOSTIC KITK862969 · LJM | 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
