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 15, 2026, FDA's public records list Bridger Biomed with 7 510(k) clearances. The most recent is a 510(k) clearance dated Jan 26, 2001: MODIFICATION TO FLUOROTEX II SURGICAL MESH.
| Jan 26, 2001 | MODIFICATION TO FLUOROTEX II SURGICAL MESHK003917 · FTL | 510(k) clearances |
| Jan 26, 2001 | MODIFICATION TO FLUROTEX SURGICAL MESHK003906 · FTL | 510(k) clearances |
| Aug 26, 2000 | FLUOROTEX II SURGICAL MESHK002351 · FTL | 510(k) clearances |
| Jul 7, 2000 | FLUORO-TEX CARDIOVASCULAR PATCHK994032 · DXZ | 510(k) clearances |
| Jan 7, 1999 | FLUOROTEX SURGICAL MESHK984197 · FTL | 510(k) clearances |
| May 13, 1998 | DURA-PATCH MODEL DP-XXXK980548 · GXQ | 510(k) clearances |
| Nov 24, 1997 | FLUORO-TEX SURGICAL MEMBRANEK973178 · DXZ | 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
