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Aptek, Ltd.

Country not established

Devices
2

What Aptek, Ltd. makes

Aptek, Ltd. manufactures disposable ultrasound procedure trays designed for sterile medical imaging procedures, as well as the Auto-Mate Camera, a device for capturing medical imaging outputs. These products support procedural workflows in diagnostic imaging settings.

The company’s portfolio includes Class I and Class II devices, with relevant products listed under the FDA’s 510(k) pathway. Aptek, Ltd. is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Aptek Ultrasound Procedure Tray Ref K802666

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Auto-Mate Camera Ref K803157

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

Frequently asked questions

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

The registry currently lists 2 devices for Aptek, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Aptek, Ltd.'s devices?

Among its 2 most recently registered devices, Aptek, Ltd. has devices listed in FDA 510(k) (2 devices).

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

Among its 2 most recently registered devices, the classes recorded for Aptek, Ltd.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Aptek, Ltd. include APTEK ULTRASOUND PROCEDURE TRAY and AUTO-MATE CAMERA.

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