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Techdent Technologies, Ltd.

IsraelFDA applicant, unverified

Devices
1

What Techdent Technologies, Ltd. makes

Techdent Technologies, Ltd. manufactures the APX21, a dental device designed for intraoral imaging and diagnostics, enabling high-resolution scans of oral structures.

The APX21 is classified as a Class II (U) device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • APX21 Ref K073185

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

Frequently asked questions

How many devices does Techdent Technologies, Ltd. have in the registry?

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

Which registries list Techdent Technologies, Ltd.'s devices?

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

What are the newest devices from Techdent Technologies, Ltd. in the registry?

The most recently registered devices listed for Techdent Technologies, Ltd. include APX21.

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