HomeItalyA.T.S. Applicazione Tecnologie Speciali s.r.l.

A.T.S. Applicazione Tecnologie Speciali s.r.l.

Italy · Torre De 'Roveri
✓ Record-verifiedregistrations found in 3 markets

This company has registrations in United States, Canada, Russia — 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
3listed device types
Class I 0Class II 3Class III 0
plus 4 registration records and 4 510(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
0active device licences
3 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
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 States4 registration records, 4 510(k), 0 PMA
Manufacturer names merged into this page: A.T.S. Applicazione Tecnologie Speciali s.r.l. · A.T.S. APPLICAZIONE TECNOLOGIE SPECIALI S.R.L.

Company information

Country
Italy
City
Torre De 'Roveri

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

12019 · K182086
22021 · K211777
12025 · K250282

FDA listed device types

Image-Intensified Fluoroscopic X-Ray System, Mobile 1Solid State X-Ray Imager (Flat Panel/Digital Imager) 1Interventional Fluoroscopic X-Ray System 1

Registration details (sample)

MarketIdentifierNameClass / date
USK250282Persona C HR2025-04-30
USK211777ARCO FP-S2021-08-13
USK211542PRIMO S2021-07-09

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