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 13, 2026, FDA's public records list Biolucent, Inc. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Apr 4, 2007: BIOLUCENT APPLICATOR KIT.
| Date | Record | Source |
|---|---|---|
| Apr 4, 2007 | BIOLUCENT APPLICATOR KITK070659 · JAQ | 510(k) clearances |
| Oct 20, 2006 | BIOLUCENT APPLICATOR KITK062830 · JAQ | 510(k) clearances |
| Sep 13, 2006 | MAMMOPAD RADIOLUCENT CUSHIONK062141 · IYX | 510(k) clearances |
| Jul 28, 2006 | BIOLUCENT APPLICATOR, MODEL RTA-XXK061241 · JAQ | 510(k) clearances |
| Feb 28, 2006 | CURAY CUSTOM SEED ARRAYK053595 · KXK | 510(k) clearances |
| Feb 14, 2001 | BIOLUCENT MAMMOGRAPHY CUSHIONK003795 · IZH | 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
