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., part of BDLabelled 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 IMPRA with 29 510(k) clearances. The most recent is a 510(k) clearance dated May 14, 2001: IMPRA CARBOFLO EPTFE VASCULAR GRAFTS.
| May 14, 2001 | IMPRA CARBOFLO EPTFE VASCULAR GRAFTSK004012 · DYF | 510(k) clearances |
| Mar 27, 2001 | IMPRA CARBOFLO VASCULAR GRAFT, IMPRA CARBOFLO VASCULAR GRAFTS FOR A-V ACCESSK004011 · DSY | 510(k) clearances |
| Apr 22, 1999 | BI-DIRECTIONAL TUNNELERK991027 · DSY | 510(k) clearances |
| Dec 15, 1998 | DISTAFLO BYPASS GRAFTK983769 · DYF | 510(k) clearances |
| Nov 24, 1998 | DISTAFLO BYPASS GRAFTK983861 · DSY | 510(k) clearances |
| Nov 19, 1998 | IMPRA HIGH POROSITY GRAFTK983064 · DSY | 510(k) clearances |
| May 7, 1998 | VENAFLO PTFE VASCULAR GRAFT, VENAFLO GRAFT WITH CARBON, VENAFLO VASCULAR GRAFTK981079 · DSY | 510(k) clearances |
| May 7, 1998 | VENAFLO PTFE VASCULAR GRAFT, VENAFLO GRAFT WITH CARBON, VENAFLO VASCULAR GRAFTK981076 · DYF | 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
