Nico Corporation is one of 17045 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nico Corporation - FDA 510(k) Cleared Devices
Recent clearances: Myriad SPECTRA Light Source, NICO Myriad NOVUS, NICO Myriad
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.
Regulatory submissions have been managed by Underwriters Laboratories, Inc. and Regulatory Technology Services, LLC.
FDA 510(k) Regulatory Record - 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