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Grove Video Corp.

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Devices
1

What Grove Video Corp. makes

Grove Video Corp. manufactures the TP440 OrthoProbe, a device designed for orthopedic assessment and surgical guidance, likely used in joint or bone procedures to aid precision and accuracy during procedures.

The TP440 OrthoProbe is classified as a Class II medical 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, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • TP440 Orthoprobe Ref K821571

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

Frequently asked questions

How many devices does Grove Video Corp. have in the registry?

The registry currently lists 1 device for Grove Video Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Grove Video Corp.'s devices?

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

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

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

What are the newest devices from Grove Video Corp. in the registry?

The most recently registered devices listed for Grove Video Corp. include TP440 ORTHOPROBE.

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