HomeUSANICO CORPORATION

NICO CORPORATION

USA · Indianapolis
✓ Record-verifiedregistrations found in 5 markets

This company has registrations in United States, Canada, Singapore, Australia, Israel — 5 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable
CNChinaNMPA
n/aThis registry lists domestic registrants only
EUEuropean UnionEUDAMED
pendingnot queried
USUnited StatesFDA openFDA
17listed device types
Class I 9Class II 8Class III 0
plus 15 registration records and 9 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
0registered devices
this export covers Class I / II only (the cadastro route)
SASaudi ArabiaSFDA
0registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
5 including historic records
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
2device registrations
CLASS D 2
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
23active ARTG entries
Class I 9Class III 6IIa 2IIb 1Class Is (sterile) 5
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
1registrations
RURussiaRoszdravnadzor
pendingnot queried
Not yet connected: India CDSCO, Indonesia Kemenkes. The public search for Japan PMDA and Vietnam IMDA does not return manufacturer names, so entries cannot be linked to companies coming — where there is no data it is shown as "pending", never estimated.

How these numbers were verified

record-verified

Company-name search in every official database is a substring match and returns same-named but different companies. Each figure below is the count after re-checking every record against the manufacturer name.

United States15 registration records, 9 510(k), 0 PMA, 3 excluded
Manufacturer names merged into this page: NICO CORPORATION

Company information

Country
USA
City
Indianapolis

Fields marked "pending" have not been obtained yet; that does not mean they do not exist. Risk records (litigation, penalties, operating anomalies) are kept internal and not published.

FDA 510(k) clearances by year

12012
22015
22016
12017
12018
12019
12024

FDA listed device types

showing 8 of 17
Electrosurgical, Cutting & Coagulation & Accessories 1Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece 1Retractor, Self-Retaining, For Neurosurgery 1Diagnostic Neurosurgical Microscope Filter 1Motor, Drill, Electric 1Light, Surgical, Fiberoptic 1Tube, Aspirating, Flexible, Connecting 1Illuminator, Fiberoptic, Surgical Field 1

Registration details (sample)

MarketIdentifierNameClass / date
USK232567Myriad SPECTRA Light Source2024-03-14
USK191599NICO Myriad NOVUS2019-09-13
USK182340NICO Myriad2018-09-20

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