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H.B.M. USA Co., Inc.

Country not established

Devices
1

What H.B.M. USA Co., Inc. makes

H.B.M. USA Co., Inc. manufactures powdered and powder-free surgeons' gloves, designed for use in sterile surgical procedures to maintain hygiene and reduce contamination risk during operations.

These products are classified as Class I medical devices 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.

Catalogue1

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Frequently asked questions

How many devices does H.B.M. USA Co., Inc. have in the registry?

The registry currently lists 1 device for H.B.M. USA Co., Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list H.B.M. USA Co., Inc.'s devices?

Among its 1 most recently registered device, H.B.M. USA Co., Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do H.B.M. USA Co., Inc.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for H.B.M. USA Co., Inc.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from H.B.M. USA Co., Inc. in the registry?

The most recently registered devices listed for H.B.M. USA Co., Inc. include MEDISPO (POWDERED) AND MEDISPO-PF (POWDER-FREE) SURGEONS GLOVE.

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