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Tuco Innovations, Inc.

Country not established

Devices
1

What Tuco Innovations, Inc. makes

Tuco Innovations, Inc. manufactures the ERCHONIA PL2000, a device intended for use in medical imaging, specifically designed for photodynamic therapy applications.

The ERCHONIA PL2000 is classified as a Class II medical device 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

Newest first, rows 1-1 of 1

  • Erchonia PL2000 Ref K012580

    Class II
    Active 510(k) 510(k) II

Frequently asked questions

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

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

Which registries list Tuco Innovations, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Tuco Innovations, Inc. include ERCHONIA PL2000.

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