Medical Device Manufacturer · US , Indianapolis , IN

Nico Corporation

9 submissions · 9 cleared · Since 2012
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.

9 devices
1–9 of 9
Myriad SPECTRA Light Source
K232567 · QFX Diagnostic Neurosurgical Microscope Filter · Neurology
Mar 2024 203d
NICO Myriad NOVUS
K191599 · GEI Electrosurgical, Cutting & Coagulation & Accessories · Obstetrics & Gynecology
Sep 2019 88d
NICO Myriad
K182340 · GEI Electrosurgical, Cutting & Coagulation & Accessories · Obstetrics & Gynecology
Sep 2018 23d
NICO BrainPath
K172433 · GZT Retractor, Self-retaining, For Neurosurgery · Neurology
Sep 2017 27d
NICO Myriad
K161307 · GEI Electrosurgical, Cutting & Coagulation & Accessories · Obstetrics & Gynecology
Dec 2016 225d
NICO TRIOwand
K162075 · GEI Electrosurgical, Cutting & Coagulation & Accessories · General & Plastic Surgery
Aug 2016 15d
NICO BrainPath & Accessories, NICO BrainPath, NICO Shepherd's Hook
K150378 · GZT Retractor, Self-retaining, For Neurosurgery · Neurology
Jun 2015 119d
NICO TRIOwand
K150993 · GEI Electrosurgical, Cutting & Coagulation & Accessories · General & Plastic Surgery
Apr 2015 8d
BRAIN PORT
K120691 · GZT Retractor, Self-retaining, For Neurosurgery · Neurology
Jun 2012 90d
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All9 Neurology 4 Obstetrics & Gynecology 3 General & Plastic Surgery 2