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Precision Neuroscience, Corp.

Country not established

Devices
1

What Precision Neuroscience, Corp. makes

Precision Neuroscience, Corp. manufactures the Layer 7-T, a device designed for targeted neurosurgical applications, likely involving deep brain stimulation or neuromodulation systems.

The Layer 7-T is classified as a Class II medical 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, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Layer 7-T Ref K242618

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

Frequently asked questions

How many devices does Precision Neuroscience, Corp. have in the registry?

The registry currently lists 1 device for Precision Neuroscience, Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Precision Neuroscience, Corp.'s devices?

Among its 1 most recently registered device, Precision Neuroscience, Corp. has devices listed in FDA 510(k) (1 device).

What risk classes do Precision Neuroscience, Corp.'s devices fall under?

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

What are the newest devices from Precision Neuroscience, Corp. in the registry?

The most recently registered devices listed for Precision Neuroscience, Corp. include Layer 7-T.

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