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Anestech, Inc.

Country not established

Devices
1

What Anestech, Inc. makes

Anestech, Inc. manufactures the ANESTHASSIST, a device designed to assist in anesthesia administration and monitoring during medical procedures.

The ANESTHASSIST is classified as a Class I medical device under FDA regulations and is listed in the FDA’s 510(k) clearance database. The company is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Anesthassist Ref K871564

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

Frequently asked questions

How many devices does Anestech, Inc. have in the registry?

The registry currently lists 1 device for Anestech, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Anestech, Inc.'s devices?

Among its 1 most recently registered device, Anestech, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Anestech, Inc.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Anestech, Inc.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Anestech, Inc. in the registry?

The most recently registered devices listed for Anestech, Inc. include ANESTHASSIST.

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