Baxano, Inc. is one of 18375 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Baxano, Inc. - FDA 510(k) Cleared Devices
Recent clearances: IO-TOME DEVICE, NEURO CHECK DEVICE WITH IO-FLEX WIRE, NEURO CHECK DEVICE WITH IO-FLEX WIRE
10
Total
10
Cleared
0
Denied
Baxano, Inc. has 10 FDA 510(k) cleared medical devices. Based in Yorba Linda, US.
Historical record: 10 cleared submissions from 2007 to 2012. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Baxano, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Baxano, Inc.
10 devices
Cleared
Jul 27, 2012
IO-TOME DEVICE
Neurology
284d
Cleared
Apr 11, 2012
NEURO CHECK DEVICE WITH IO-FLEX WIRE
Neurology
133d
Cleared
Jul 07, 2011
NEURO CHECK DEVICE WITH IO-FLEX WIRE
Ear, Nose, Throat
115d
Cleared
Jan 19, 2011
IO-FLEX CATHETER
Anesthesiology
132d
Cleared
Jul 23, 2010
MODIFICATION TO: MICROBLADE SHAVER AND ACCESSORIES
Neurology
107d
Cleared
Oct 02, 2009
BAXANO NEURO CHECK DEVICE
Ear, Nose, Throat
28d
Cleared
Sep 17, 2008
BAXANO NEURAL LOCALIZATION PROBE 1.75 AND 1.25
Ear, Nose, Throat
90d
Cleared
Mar 04, 2008
BAXANO ULTRA LOW PROFILE RONGEUR
Neurology
11d
Cleared
Apr 16, 2007
MICROBLADE SHAVER AND ACCESSORIES
Neurology
173d
Cleared
Mar 07, 2007
ULTRA LOW PROFILE RONGEUR
Neurology
177d