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Avratronics Corp.

United StatesFDA 510(k) applicant, unverified

Devices
2

What Avratronics Corp. makes

Avratronics Corp. manufactures the GALVANATOR 725, an electrotherapy device, and the ACRATRAC R, a traction system for musculoskeletal applications. These products are designed for therapeutic interventions in clinical settings, including electrical stimulation and mechanical traction therapies.

The company’s portfolio includes devices classified as Class I and Class II under FDA regulations, with submissions recorded in the 510(k) clearance pathway. The manufacturer is based in the United States.

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

Catalogue2

Newest first, rows 1-2 of 2

  • Galvanator 725 Ref K810057

    Class II
    Active 510(k) 510(k) II
  • Acratrac R Ref K811438

    Class I
    Active 510(k) 510(k) I

Frequently asked questions

How many devices does Avratronics Corp. have in the registry?

The registry currently lists 2 devices for Avratronics Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Avratronics Corp.'s devices?

Among its 2 most recently registered devices, Avratronics Corp. has devices listed in FDA 510(k) (2 devices).

What risk classes do Avratronics Corp.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Avratronics Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Avratronics Corp. in the registry?

The most recently registered devices listed for Avratronics Corp. include GALVANATOR 725 and ACRATRAC R.

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