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 14, 2026, FDA's public records list Flexible Stenting Solutions with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jul 6, 2012: FLEXSTENT BILIARY SELF-EXPANDING STENT SYSTEM.
| Jul 6, 2012 | FLEXSTENT BILIARY SELF-EXPANDING STENT SYSTEMK121125 · FGE | 510(k) clearances |
| Apr 24, 2012 | FLEXSTENT BILIARY SELF-EXPANDING STENT SYSTEMK120452 · FGE | 510(k) clearances |
| Dec 30, 2011 | FLEXSTENT BILIARY SELF-EXPANDING STENT SYSTEMK112522 · FGE | 510(k) clearances |
| Nov 22, 2010 | FLEXSTENT BILIARY SELF EXPANDING STENT SYSTEM MODEL FLX-DDLLL-BXK102519 · FGE | 510(k) clearances |
| Sep 15, 2009 | FLEXSTENT BILIARY SELF EXPANDING STENT SYSTEMK081996 · 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
