HomeUSAEYEKON MEDICAL, INC.

EYEKON MEDICAL, INC.

USA · Clearwater
✓ Record-verifiedregistrations found in 3 markets

This company has registrations in United States, Canada, Israel — 3 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
6listed device types
Class I 1Class II 1Class III 4
plus 7 registration records and 1 510(k), 32 PMA
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
1active device licences
Class III 1
TWTaiwanTFDA
0valid device licences
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
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 States7 registration records, 1 510(k), 32 PMA
Canada1 confirmed, 0 excluded
Manufacturer names merged into this page: EYEKON MEDICAL, INC. · EYEKON MEDICAL INC.

Company information

Country
USA
City
Clearwater

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

12026 · K261312

FDA listed device types

Intraocular Lens 1Lens, Multifocal Intraocular 1Aid, Surgical, Viscoelastic 1Ring, Endocapsular 1Keratoprosthesis, Temporary Implant, Surgical Use 1Folders And Injectors, Intraocular Lens (Iol) 1

Registration details (sample)

MarketIdentifierNameClass / date
USK261312Temporary Keratoprosthesis (QuickSet TKP™)2026-07-24
CA62319PMMA SINGLE INTRAOCULAR LENSESClass III

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