Nico Corporation - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Nico Corporation has 9 FDA 510(k) cleared medical devices. Based in Indianapolis, US.
Latest FDA clearance: Mar 2024. Active since 2012. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Nico Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Nico Corporation
9 devices
Cleared
Mar 14, 2024
Myriad SPECTRA Light Source
Neurology
203d
Cleared
Sep 13, 2019
NICO Myriad NOVUS
Obstetrics & Gynecology
88d
Cleared
Sep 20, 2018
NICO Myriad
Obstetrics & Gynecology
23d
Cleared
Sep 07, 2017
NICO BrainPath
Neurology
27d
Cleared
Dec 21, 2016
NICO Myriad
Obstetrics & Gynecology
225d
Cleared
Aug 11, 2016
NICO TRIOwand
General & Plastic Surgery
15d
Cleared
Jun 12, 2015
NICO BrainPath & Accessories, NICO BrainPath, NICO Shepherd's Hook
Neurology
119d
Cleared
Apr 23, 2015
NICO TRIOwand
General & Plastic Surgery
8d
Cleared
Jun 05, 2012
BRAIN PORT
Neurology
90d