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Etzem Technologies, Inc.

IsraelFDA 510(k) applicant, unverified

Devices
1

What Etzem Technologies, Inc. makes

Etzem Technologies, Inc. manufactures the FREEDLAND TENSION SYSTEM, a device designed for orthopedic applications to manage tension in surgical procedures, such as ligament reconstruction or tendon repair.

The FREEDLAND TENSION SYSTEM is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.

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

Catalogue1

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Frequently asked questions

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

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

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

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

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

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

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

The most recently registered devices listed for Etzem Technologies, Inc. include FREEDLAND TENSION SYSTEM.

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