HomeIndiaFORUS HEALTH PVT.LTD.

FORUS HEALTH PVT.LTD.

India · Bangalore
✓ Record-verifiedregistrations found in 6 markets

This company has registrations in United States, Brazil, Canada, Australia, Israel, Russia — 6 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 2Class II 4Class III 0
plus 7 registration records and 2 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
1registered devices
Class II 1
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
3 including historic records
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
1active ARTG entries
Class I 1
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
1registrations
RURussiaRoszdravnadzor
1active registrations
Class 2a 1
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, 2 510(k), 0 PMA
Brazil1 confirmed, 0 excluded
Manufacturer names merged into this page: FORUS HEALTH PVT.LTD., · FORUS HEALTH PVT LTD. · FORUS HEALTH PUT LTD

Company information

Country
India
City
Bangalore

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

12018 · K183059
12025 · K243600

FDA listed device types

Refractor, Manual, Non-Powered, Including Phoropter 1Refractometer, Ophthalmic 1Camera, Ophthalmic, General-Use 1Photorefractor 1Camera, Ophthalmic, Ac-Powered 1Biomicroscope, Slit-Lamp, Ac-Powered, Exempt 1

Registration details (sample)

MarketIdentifierNameClass / date
USK2436003nethra neo HD FA; 3nethra neo HD2025-08-14
USK1830593nethra neo2018-12-21
BR813465090783nethra neo – Sistema de Imagem retiniana pediátricaClass II

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