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Grad-Line Corp.

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Devices
1

What Grad-Line Corp. makes

Grad-Line Corp. manufactures the ATLANT'S, a medical device designed for spinal cord stimulation and pain management applications, targeting chronic pain conditions through electrical signal modulation.

The ATLANT'S is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. 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

  • Atlant's Ref K974395

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

Frequently asked questions

How many devices does Grad-Line Corp. have in the registry?

The registry currently lists 1 device for Grad-Line Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Grad-Line Corp.'s devices?

Among its 1 most recently registered device, Grad-Line Corp. has devices listed in FDA 510(k) (1 device).

What risk classes do Grad-Line Corp.'s devices fall under?

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

What are the newest devices from Grad-Line Corp. in the registry?

The most recently registered devices listed for Grad-Line Corp. include ATLANT'S.

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