HomeItalyDOMINO S.R.L.

DOMINO S.R.L.

Italy · Codogne Treviso
✓ Record-verifiedregistrations found in 4 markets

This company has registrations in United States, Brazil, Taiwan, Israel — 4 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
8listed device types
Class I 2Class II 6Class III 0
plus 7 registration records and 2 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
5registered devices
Class 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
1valid device licences
Class II 1
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
2registrations
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, 2 510(k), 0 PMA, 1 excluded
Brazil5 confirmed, 0 excluded
Manufacturer names merged into this page: DOMINO S.R.L.

Company information

Country
Italy
City
Codogne Treviso

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

22007 · K071431

FDA listed device types

Stimulator, Muscle, Powered 1Electrode, Cutaneous 1Interferential Current Therapy 1Stimulator, Muscle, Powered, For Muscle Conditioning 1Stimulator, Nerve, Transcutaneous, For Pain Relief 1Massager, Vacuum, Radio Frequency Induced Heat 1Platform, Force-Measuring 1Exerciser, Powered 1

Registration details (sample)

MarketIdentifierNameClass / date
USK071431GLOBUS GENESY 1100 STIMULATOR2007-09-21
USK061632GLOBUS PREMIUM MUSCLE STIMULATOR2007-04-30
BR81979139003EQUIPAMENTO PARA TERAPIA POR DIATERMIAClass II
BR81979130000GENESY 1200 PROClass II
BR81979130002MEDISOUNDClass II

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