Avantis Medical Systems, Inc. is one of 15062 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Avantis Medical Systems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Third Eye Panoramic Auxiliary Endoscopy System - Resposable, THIRD EYE PANORAMIC AUXILIARY ENDOSCOPY SYSTEM, MODIFICATION TO THIRD EYE RETROSCOPE AUXILIARY ENDOSCOPY SYSTEM
6
Total
6
Cleared
0
Denied
Avantis Medical Systems, Inc. has 6 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.
Historical record: 6 cleared submissions from 2007 to 2016. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Avantis Medical Systems, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Avantis Medical Systems, Inc.
6 devices
Cleared
May 17, 2016
Third Eye Panoramic Auxiliary Endoscopy System - Resposable
Gastroenterology & Urology
99d
Cleared
Nov 17, 2014
THIRD EYE PANORAMIC AUXILIARY ENDOSCOPY SYSTEM
Gastroenterology & Urology
255d
Cleared
Nov 05, 2009
MODIFICATION TO THIRD EYE RETROSCOPE AUXILIARY ENDOSCOPY SYSTEM
Gastroenterology & Urology
27d
Cleared
Jul 07, 2009
THIRD EYE RETROSCOPE AUXILIARY ENDOSCOPE SYSTEM
Gastroenterology & Urology
20d
Cleared
Feb 12, 2009
THIRD EYE RETROSCOPE AUXILIARY ENDOSCOPY SYSTEM
Gastroenterology & Urology
107d
Cleared
Apr 24, 2007
THIRD EYE RETROSCOPE AUXILIARY ENDOSCOPY SYSTEM
Gastroenterology & Urology
78d