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 Alexon with 10 510(k) clearances. The most recent is a 510(k) clearance dated Sep 20, 1994: PROSPECT MICROPLATE ASSAY.
| Sep 20, 1994 | PROSPECT MICROPLATE ASSAYK934493 · LLH | 510(k) clearances |
| Sep 9, 1994 | PROSPECT GIARDIAK942098 · MHI | 510(k) clearances |
| May 13, 1993 | PROSPECT(TM) GIARDIA RAPID ASSAY, MODIFICATIONK931147 · MHI | 510(k) clearances |
| Apr 21, 1993 | PROSPEC T GIARDIA MICROTITER ASSAYK930451 · MHI | 510(k) clearances |
| Sep 11, 1992 | PROSPECT GIARDIA CONTROLSK922675 · MHI | 510(k) clearances |
| Jun 19, 1992 | PROSPECT(TM) GIARDIA MICROTITER ASSAY/MODIFICATIONK922010 · MHI | 510(k) clearances |
| Apr 22, 1992 | MODIFICATION PROSPECT GIARDIA RAPID ASSAYK920817 · MHI | 510(k) clearances |
| Mar 23, 1992 | PROSPECT(TM/CRYPTOSPORIDIUMK912242 · MHJ | 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
