Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 Bioject with 9 510(k) clearances. The most recent is a 510(k) clearance dated Apr 2, 2009: ZETAJET.
| Date | Record | Source |
|---|---|---|
| Apr 2, 2009 | ZETAJETK090003 · KZE | 510(k) clearances |
| Jun 3, 2005 | COOL.CLICKK050734 · KZE | 510(k) clearances |
| Apr 5, 2001 | RECONSTITUTION KIT & VIAL CONNECTORK010623 · LHI | 510(k) clearances |
| Mar 8, 2001 | SEROJETK003908 · KZE | 510(k) clearances |
| Jun 22, 2000 | CLICKERK994384 · KZE | 510(k) clearances |
| Mar 5, 1997 | BIOJECTOR 2000 MODEL 1B02000K960373 · KZE | 510(k) clearances |
| Oct 15, 1996 | BIOJECT NEEDLE-FREE VIAL ADAPTER (13MM)K963012 · LHI | 510(k) clearances |
| Jun 28, 1994 | BIOJECT JET INJECTION SYSTEMK920631 · KZE | 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
