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 15, 2026, FDA's public records list Orbus Medical Technologies with 8 510(k) clearances. The most recent is a 510(k) clearance dated Jun 24, 2004: LIFESTENT LP SDS BILIARY ENDOPROSTHESIS.
| Jun 24, 2004 | LIFESTENT LP SDS BILIARY ENDOPROSTHESISK041370 · FGE | 510(k) clearances |
| May 10, 2004 | MODIFICATION TO LIFESTENT SDS AND XL SDS BILIARY ENDOPROSTHESISK041032 · FGE | 510(k) clearances |
| Mar 16, 2004 | LIFESTENT SDS AND XL SDS BILIARY ENDOPROSTHESISK040550 · FGE | 510(k) clearances |
| Oct 30, 2003 | LIFESTENT SDS BILIARY ENDOPROSTHESISK033212 · FGE | 510(k) clearances |
| Apr 14, 2003 | LIFESTENT SDS BILIARY ENDOPROSTHESIS, LIFESTENT XL SDS BILIARY ENDOPROSTHESISK023308 · FGE | 510(k) clearances |
| Mar 10, 2003 | LIFESTENT BILIARY ENDOPROSTHESISK023121 · FGE | 510(k) clearances |
| Feb 11, 2003 | LIFESTENT LP SDS BILIARY ENDOPROSTHESISK023248 · FGE | 510(k) clearances |
| Jul 31, 2001 | R STENT BILIARY ENDOPROSTHESISK010107 · FGE | 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
