HomeFranceMETROVISION SAS

METROVISION SAS

France · Perenchies
✓ Record-verifiedregistrations found in 5 markets

This company has registrations in United States, Canada, Australia, Israel, Russia — 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
6listed device types
Class I 4Class II 2Class III 0
plus 6 registration records and 2 510(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
4active device licences
Class II 4
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
1active ARTG entries
IIa 1
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
2registrations
RURussiaRoszdravnadzor
2active registrations
Class 2a 2
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 States6 registration records, 2 510(k), 0 PMA
Canada4 confirmed, 0 excluded
Manufacturer names merged into this page: METROVISION SAS · METROVISION

Company information

Country
France
City
Perenchies

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

12021 · K211643
12022 · K212936

FDA listed device types

Stimulator, Photic, Evoked Response 1Preamplifier, Ac-Powered, Ophthalmic 1Perimeter, Automatic, Ac-Powered 1Pupillometer, Ac-Powered 1Adaptometer (Biophotometer), Software-Based Data Acquisition And Stimulus Generation 1Chart, Visual Acuity 1

Registration details (sample)

MarketIdentifierNameClass / date
USK212936Vision Monitor- MonCvONE2022-11-21
USK211643Vision Monitor - MonpackONE2021-07-26
CA75213VISION MONITOR HARDWARESClass II
CA75464BIOELECTRIC AMPLIFIERSClass II
CA75465VISION MONITOR SOFTWARESClass II

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