EU → North America Device Access

INDUSTRIA ZINGARDI S.R.L.

IT-MF-000041566 · Italy · NOVI LIGURE (AL)

INDUSTRIA ZINGARDI S.R.L. is registered in the European database on medical devices as a manufacturer, with 36 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

Class IIa36

Most frequent device types declared: FDE2000.

Devices declared under this manufacturer

Showing 12 of 36 declared devices.

Catalogue references include 138/500RA, 139/500GA, 155/44AZ, 165/96RS, 168/24GA, 380/24VE.

European nomenclature codes declared: Q01020203, Q010499, Q010299.

United States market access

FDA establishment registerRegistered with FDA
Matched entryINDUSTRIA ZINGARDI S.R.L (IT) · FDA 3008960188
Devices in EUDAMED36
Country of registrationItaly

Device-level evidence

Devices with a numeric GTIN36
Found in the U.S. device database0
Share0.0 %

Canadian market access

Health Canada licence listingLicensed in Canada
Matched entryINDUSTRIA ZINGARDI S.R.L

What it holds in Canada

Licences on record1
Currently active0
Class 2 devices1
First licensed2025-10-22

Licence types: Single Device (1).

Licensed under: CURAPROX HYDROSONIC PRO.

North American profile: Both markets. INDUSTRIA ZINGARDI S.R.L. is registered in both the United States and Canada.

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