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Thornton Associates, Inc.

United StatesFDA applicant, unverified

Devices
2

What Thornton Associates, Inc. makes

Thornton Associates, Inc. manufactures the IPG-300, a medical device designed for implantable pulse generator applications, and the SPIRAL, a device used in neurostimulation procedures. These products are intended for targeted electrical stimulation in therapeutic settings.

The company’s portfolio is regulated under Class II medical devices in the US, with devices listed via FDA 510(k) clearance. Thornton Associates, Inc. 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

  • Ipg-300 Ref K852238

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

  • Spiral Ref K920514

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

Frequently asked questions

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

The registry currently lists 2 devices for Thornton Associates, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Thornton Associates, Inc.'s devices?

Among its 2 most recently registered devices, Thornton Associates, Inc. has devices listed in FDA 510(k) (2 devices).

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

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

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

The most recently registered devices listed for Thornton Associates, Inc. include IPG-300 and SPIRAL.

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