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Leibinger L.P.

Country not established

Devices
1

What Leibinger L.P. makes

Leibinger L.P. manufactures spinal markers, which are used to assist in surgical navigation and alignment during spinal procedures.

The company’s products are regulated as Class I medical devices in the U.S. and are listed under the FDA’s 510(k) pathway. The manufacturer 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

  • Spinal Marker Ref K944188

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

Frequently asked questions

How many devices does Leibinger L.P. have in the registry?

The registry currently lists 1 device for Leibinger L.P.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Leibinger L.P.'s devices?

Among its 1 most recently registered device, Leibinger L.P. has devices listed in FDA 510(k) (1 device).

What risk classes do Leibinger L.P.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Leibinger L.P.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Leibinger L.P. in the registry?

The most recently registered devices listed for Leibinger L.P. include SPINAL MARKER.

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