Entellus Medical, Inc. - FDA 510(k) Cleared Devices
27
Total
27
Cleared
0
Denied
Entellus Medical, Inc. has 27 FDA 510(k) cleared ear, nose, throat devices. Based in Maple Grove, US.
Last cleared in 2022. Active since 2008.
Browse the complete list of FDA 510(k) cleared ear, nose, throat devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Entellus Medical, Inc.
27 devices
Cleared
Apr 12, 2022
Audion ET dilation system
Ear, Nose, Throat
97d
Cleared
Apr 05, 2017
Entellus Medical Reinforced Anesthesia Needle
Anesthesiology
119d
Cleared
Apr 05, 2017
XprESS ENT Dilation System
Ear, Nose, Throat
111d
Cleared
Nov 20, 2015
XprESS Multi-Sinus Dilation System
Ear, Nose, Throat
85d
Cleared
Nov 20, 2015
PassAssist LED Light Fiber
Ear, Nose, Throat
85d
Cleared
Oct 17, 2014
XprESS Multi-Sinus Dilation Tool
Ear, Nose, Throat
64d
Cleared
Aug 07, 2014
PATHASSIST LED LIGHT FIBER
Ear, Nose, Throat
23d
Cleared
Dec 20, 2013
PATHASSIST LIGHT SEEKER
Ear, Nose, Throat
30d
Cleared
Oct 04, 2013
XPRESS MULTI-SINUS DILATION TOOL
Ear, Nose, Throat
59d
Cleared
Jun 11, 2013
PATHASSIST LED LIGHT FIBER
Ear, Nose, Throat
104d
Cleared
Aug 22, 2012
XPRESS MULTI-SINUS DILATION TOOL
Ear, Nose, Throat
50d
Cleared
May 17, 2012
XPRESS MULTI-SINUS DILATION TOOL
Ear, Nose, Throat
30d