Endoscopic Technologies, Inc. D/B/A Estech is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Endoscopic Technologies, Inc. D/B/A Estech - FDA 510(k) Cleared Devic...
5
Total
5
Cleared
0
Denied
Endoscopic Technologies, Inc. D/B/A Estech has 5 FDA 510(k) cleared medical devices. Based in San Ramon, US.
Historical record: 5 cleared submissions from 2009 to 2012. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Endoscopic Technologies, Inc. D/B/A Estech Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Endoscopic Technologies, Inc. D/B/A Estech
5 devices
Cleared
Mar 20, 2012
ESTECH COBRA ADHERE XL 2 SURGICAL SYSTEM
Cardiovascular
119d
Cleared
Sep 23, 2011
ESTECH COBRA SURGICAL SYSTEM WITH THERMASHIELD ACCESSORY
Cardiovascular
175d
Cleared
Apr 07, 2010
ESTECH COBRA BIPOLSR II
General & Plastic Surgery
71d
Cleared
Oct 20, 2009
ESTECH EASYFLOW CANNULA WITH GUIDEWIRE
Cardiovascular
147d
Cleared
Sep 15, 2009
ESTECH HAWKEYE INTRODUCER SYSTEMS
General & Plastic Surgery
131d