# Endoscopic Technologies, Inc. D/B/A Estech

- Location (FDA's records): San Ramon, CA
- FDA decisions: 5 (2009–2012): 5 510(k) clearances
- Product codes: OCL (2), GEI (1), GCJ (1), DWF (1)
- Predicates its devices cite: 9 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 5 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Endoscopic Technologies, Inc.: 2 (https://510kreport.com/company/endoscopic-technologies)
- Estech, Inc.: 2 (https://510kreport.com/company/estech)
- Boston Scientific Corp: 1 (https://510kreport.com/company/boston-scientific)
- AtriCure, Inc.: 1 (https://510kreport.com/company/atricure)
- Medtronic Cardiac Surgical Products: 1 (https://510kreport.com/company/medtronic-cardiac-surgical-products)
- Edwards Lifesciences Research Medical: 1 (https://510kreport.com/company/edwards-lifesciences-research-medical)
- Coombs Medical Device Consulting: 1 (https://510kreport.com/company/coombs-medical-device-consulting)

## Firms that cite its devices most
- Sorin Group Italia S.R.L.: 1 (https://510kreport.com/company/sorin-group-italia)
- Ncontact Surgical, Inc.: 1 (https://510kreport.com/company/ncontact-surgical)
- AtriCure, Inc.: 1 (https://510kreport.com/company/atricure)
- Estech, Inc.: 1 (https://510kreport.com/company/estech)

## Its most-cited devices
- K113475: Estech Cobra Adhere XL 2 Surgical System (2012), cited by 2
- K100224: Estech Cobra Bipolsr II (2010), cited by 1
- K091542: Estech Easyflow Cannula with Guidewire (2009), cited by 1

## Recent decisions
- K113475: Estech Cobra Adhere XL 2 Surgical System (Mar 20, 2012)
- K110913: Estech Cobra Surgical System with Thermashield Accessory (Sep 23, 2011)
- K100224: Estech Cobra Bipolsr II (Apr 7, 2010)
- K091542: Estech Easyflow Cannula with Guidewire (Oct 20, 2009)
- K091350: Estech Hawkeye Introducer Systems (Sep 15, 2009)

Source page: https://510kreport.com/company/endoscopic-technologies-d-b-a-estech