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Impertech Industries, Ltd.

IsraelFDA applicant, unverified

Devices
1

What Impertech Industries, Ltd. makes

Impertech Industries, Ltd. manufactures the Impertech Surgical Face Mask, a disposable barrier device designed for single-use in surgical and clinical settings to reduce the risk of airborne pathogen transmission.

The company’s product portfolio is regulated under FDA’s Class II device classification and requires 510(k) clearance. The device is listed in the FDA’s 510(k) database.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Impertech Surgical Face Mask Ref K212046

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Impertech Industries, Ltd. have in the registry?

The registry currently lists 1 device for Impertech Industries, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Impertech Industries, Ltd.'s devices?

Among its 1 most recently registered device, Impertech Industries, Ltd. has devices listed in FDA 510(k) (1 device).

What risk classes do Impertech Industries, Ltd.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Impertech Industries, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Impertech Industries, Ltd. in the registry?

The most recently registered devices listed for Impertech Industries, Ltd. include Impertech Surgical Face Mask.

Generated automatically from registry data and not verified by a human reviewer.