Diagnostics 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 Bionetic Laboratory Products with 8 510(k) clearances. The most recent is a 510(k) clearance dated Feb 10, 1984: VZV BIO-ENZABEAD SCREEN KIT.
| Feb 10, 1984 | VZV BIO-ENZABEAD SCREEN KITK833637 · LFY | 510(k) clearances |
| Nov 14, 1983 | IMMUNOENZYME TEST SYS-DETECT-IGM ANTIK832900 · GLZ | 510(k) clearances |
| Sep 26, 1983 | TOXO IPA KIT IAN INDIRECT FLUORESCENTK832069 · LJK | 510(k) clearances |
| Aug 8, 1983 | LEGIONELLA IFA KIT IK831760 · LHL | 510(k) clearances |
| Jun 8, 1983 | LEGIONELLA DFA KIT IK830820 · LHL | 510(k) clearances |
| Jun 8, 1983 | AMEBIASIS BIO-ENZABEAD SCREEN KITK831133 · KHW | 510(k) clearances |
| Mar 10, 1983 | LBI-100 37DEGREES INCUBATORK830405 · JTQ | 510(k) clearances |
| Mar 10, 1983 | AUTOMATED ELISA READER LBI 300K830227 · JTQ | 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
