Skip to content

Enroxtech, Inc.

Country not established

Devices
1

What Enroxtech, Inc. makes

Enroxtech, Inc. manufactures the ENDO-CORD, a medical device designed for endoscopic procedures, likely used in cord or tissue manipulation within minimally invasive surgeries.

The ENDO-CORD is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. 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

  • Endo-Cord Ref K141330

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

Frequently asked questions

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

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

Which registries list Enroxtech, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Enroxtech, Inc. include ENDO-CORD.

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