HomeItalyESPANSIONE MARKETING SPA

ESPANSIONE MARKETING SPA

Italy · Crevalcore Bologna
✓ Record-verifiedregistrations found in 3 markets

This company has registrations in United States, Brazil, Canada — 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 5Class III 0
plus 10 registration records and 3 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
3registered devices
Class II 3
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
4 including historic records
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 States10 registration records, 3 510(k), 0 PMA
Brazil3 confirmed, 0 excluded
Manufacturer names merged into this page: ESPANSIONE MARKETING SPA · ESPANSIONE MARKETING S.P.A.

Company information

Country
Italy
City
Crevalcore Bologna

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

12007 · K070494
12010 · K092734
12013 · K124064

FDA listed device types

Pad, Heating, Powered 1Light Based Over The Counter Wrinkle Reduction 1Camera, Ophthalmic, General-Use 1Powered Laser Surgical Instrument 1Laser, Comb, Hair 1Massager, Therapeutic, Electric 1

Registration details (sample)

MarketIdentifierNameClass / date
USK124064YOUNG AGAIN2013-12-19
USK092734E-LIGHT LINE2010-09-20
USK070494EPI-C PLUS2007-05-01
BR10161029005ME-CHECKClass II
BR81346509086Sistema de FotobioestimulaçãoClass II
BR10161029006Eye-LightClass II

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