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Rhino Mfg.

Country not established

Devices
2

What Rhino Mfg. makes

Rhino Mfg. produces spinal positioning frames and headrests designed for patient support during medical procedures, including orthopedic and spinal surgeries.

These devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. The company 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

  • Spinal Positioning Frame Ref K922371

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Fisk Headrest Ref K924700

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

Frequently asked questions

How many devices does Rhino Mfg. have in the registry?

The registry currently lists 2 devices for Rhino Mfg.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Rhino Mfg.'s devices?

Among its 2 most recently registered devices, Rhino Mfg. has devices listed in FDA 510(k) (2 devices).

What risk classes do Rhino Mfg.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Rhino Mfg.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Rhino Mfg. in the registry?

The most recently registered devices listed for Rhino Mfg. include SPINAL POSITIONING FRAME and FISK HEADREST.

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