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 13, 2026, FDA's public records list Estech with 7 510(k) clearances. The most recent is a 510(k) clearance dated Oct 7, 2013: ESTECH COBRA(R) GENESIS BIPOLAR CLAMP.
| Date | Record | Source |
|---|---|---|
| Oct 7, 2013 | ESTECH COBRA(R) GENESIS BIPOLAR CLAMPK133017 · GEI | 510(k) clearances |
| Jan 26, 2006 | ESTECH CLEARVIEW MV ATRIAL DEPRESSORK053021 · DTS | 510(k) clearances |
| Dec 16, 2005 | REMOTE ACCESS PERFUSION (RAP) FEMORAL VENOUS CANNULAK052081 · DWF | 510(k) clearances |
| Sep 13, 2005 | COBRA SURGICAL SYSTEMK051749 · GEI | 510(k) clearances |
| Jul 27, 2004 | COBRA ADHERE SURGICAL SYSTEMK041599 · GEI | 510(k) clearances |
| Oct 22, 2003 | REMOTE ACCESS PERFUSION CANNULA LEFT AXILLARY 21 FRENCHK032632 · DWF | 510(k) clearances |
| Mar 11, 1999 | ESTECH ARTERIAL REMOTE ACCESS PERFUSION CANNULAK990573 · DXC | 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
