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Endoscopic Technologies, Inc.

United StatesFDA applicant, unverified

Devices
8

What Endoscopic Technologies, Inc. makes

Endoscopic Technologies, Inc. makes electrosurgical cutting and coagulation devices and accessories, including the ESTECH Cobra electrosurgical unit and cable, ESTECH Cobra bipolar system, and disposable electrocoagulation probes. The company also produces aortic cannulas such as the ESTECH Aortic Easy Flow Cannula, trocars, trocar/cannula combinations, and noninvasive tubing.

The devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.

AI-generated from registry data, 29 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue8

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Frequently asked questions

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

The registry currently lists 8 devices for Endoscopic Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Endoscopic Technologies, Inc.'s devices?

Among its 8 most recently registered devices, Endoscopic Technologies, Inc. has devices listed in FDA 510(k) (8 devices).

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

Among its 8 most recently registered devices, the classes recorded for Endoscopic Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Endoscopic Technologies, Inc. include ESTECH AORTIC EASY FLOW CANNULA, ELECTROSURGICAL CUTTING & COAGULATION DEVICE & ACCESSORIES, ESTECH COBRA ELECTROSURGICAL UNIT & CABLE and TROCARS.

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