Ino Therapeutics is one of 18347 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ino Therapeutics - FDA 510(k) Cleared Devices
Recent clearances: INOMAX DSIR (DELIVERY SYSTEM), INOBLENDER, INOMAX DS (DELIVERY SYSTEM)
8
Total
8
Cleared
0
Denied
Ino Therapeutics has 8 FDA 510(k) cleared medical devices. Based in Middleton, US.
Historical record: 8 cleared submissions from 2005 to 2013. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Ino Therapeutics Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ino Therapeutics
8 devices
Cleared
May 02, 2013
INOMAX DSIR (DELIVERY SYSTEM)
Anesthesiology
56d
Cleared
Nov 07, 2012
INOBLENDER
Anesthesiology
64d
Cleared
Sep 24, 2012
INOMAX DS (DELIVERY SYSTEM)
Anesthesiology
173d
Cleared
Jun 24, 2011
INOMAX DSIR (DELIVERY SYSTEM)
Anesthesiology
140d
Cleared
Apr 15, 2010
INOMAX DS
Anesthesiology
114d
Cleared
Aug 06, 2008
INOMAX DS (DELIVERY SYSTEM), MODEL 10003
Anesthesiology
166d
Cleared
Dec 14, 2006
INO THERAPEUTICS INOMAX DS (DELIVERY SYSTEM), MODEL 10003
Anesthesiology
162d
Cleared
Nov 04, 2005
INO THERAPEUTICS INOBLENDER, MODEL 10004
Anesthesiology
38d