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Geller & Bozeman

Country not established

Devices
1

What Geller & Bozeman makes

Geller & Bozeman manufactures disposable laryngoscope blades, single-use medical instruments designed for airway visualization during intubation procedures.

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

  • Disposblade Laryngoscope Ref K833133

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

Frequently asked questions

How many devices does Geller & Bozeman have in the registry?

The registry currently lists 1 device for Geller & Bozeman. Devices recorded under merged duplicate company entries are counted once.

Which registries list Geller & Bozeman's devices?

Among its 1 most recently registered device, Geller & Bozeman has devices listed in FDA 510(k) (1 device).

What risk classes do Geller & Bozeman's devices fall under?

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

What are the newest devices from Geller & Bozeman in the registry?

The most recently registered devices listed for Geller & Bozeman include DISPOSBLADE LARYNGOSCOPE.

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