Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in SpainLabelled 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 Leventon with 5 510(k) clearances. The most recent is a 510(k) clearance dated Dec 13, 2005: SPIRO-BALL.
| Date | Record | Source |
|---|---|---|
| Dec 13, 2005 | SPIRO-BALLK053149 · BWF | 510(k) clearances |
| Apr 7, 2004 | DOSI-FUSERK040752 · MEB | 510(k) clearances |
| Jun 8, 2000 | TRI-BALLK994074 · BWF | 510(k) clearances |
| Sep 8, 1995 | DOSI-FLOW, MODELS 20 & 30K952810 · FPA | 510(k) clearances |
| Apr 29, 1985 | DOSI FLOWK851058 · LDR | 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
