Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of AtriCureLabelled by claude-sonnet-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Endoscopic Technologies, Inc. with 13 510(k) clearances. The most recent is a 510(k) clearance dated Mar 20, 2012: ESTECH COBRA ADHERE XL 2 SURGICAL SYSTEM.
| Mar 20, 2012 | ESTECH COBRA ADHERE XL 2 SURGICAL SYSTEMK113475 · OCL | 510(k) clearances |
| Sep 23, 2011 | ESTECH COBRA SURGICAL SYSTEM WITH THERMASHIELD ACCESSORYK110913 · OCL | 510(k) clearances |
| Apr 7, 2010 | ESTECH COBRA BIPOLSR IIK100224 · GEI | 510(k) clearances |
| Oct 20, 2009 | ESTECH EASYFLOW CANNULA WITH GUIDEWIREK091542 · DWF | 510(k) clearances |
| Sep 15, 2009 | ESTECH HAWKEYE INTRODUCER SYSTEMSK091350 · GCJ | 510(k) clearances |
| May 10, 2006 | ESTECH AORTIC EASY FLOW CANNULAK060101 · DWF | 510(k) clearances |
| Jan 6, 2006 | ESTECH COBRA ELECTROSURGICAL UNIT & CABLEK053326 · GEI | 510(k) clearances |
| Dec 19, 2005 | ESTECH COBRA BIPOLAR SYSTEMK053100 · GEI | 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
