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Home›Brazil›PHELCOM TECHNOLOGIES S/A

PHELCOM TECHNOLOGIES S/A

Brazil
✓ Record-verifiedregistrations found in 2 markets

This company has registrations in United States, Brazil — 2 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
2listed device types
Class I 0Class II 2Class III 0
plus 3 registration records and 2 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
6registered devices
Class I 1Class II 5
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
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
pendingnot queried
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 States3 registration records, 2 510(k), 0 PMA
Brazil6 confirmed, 0 excluded
Manufacturer names merged into this page: PHELCOM TECHNOLOGIES · PHELCOM TECHNOLOGIES S/A
Same-named companies — This database also contains companies with near-identical names: PHELCOM TECHNOLOGIES. Company name alone cannot separate their registrations, so the figures below may include either.

Company information

Country
Brazil

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

12023 · K221329
12026 · K251353

FDA listed device types

Camera, Ophthalmic, General-Use 1Camera, Ophthalmic, Ac-Powered 1

Registration details (sample)

MarketIdentifierNameClass / date
USK251353Eyer 22026-01-16
USK221329Eyer Retinal Camera NM-STD2023-02-22
BR81663560003Base Acessória para ExamesClass I
BR81663569003Eyer2 PROClass II
BR81663560002EyerMapsClass II

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