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Woodside Biomedical, Inc.

United StatesFDA applicant, unverified

Devices
6

What Woodside Biomedical, Inc. makes

Woodside Biomedical, Inc. manufactures RELIEFBAND devices, including models for both MST (RB-2, RB-6, RB-R, RB-DL, RB-EL, RB-RL) and NST (WB-2, WB-6, WB-R, WB-2L, WB-6L, WB-RL) applications. These devices are designed for therapeutic compression and pressure management, targeting conditions requiring controlled external pressure therapy.

The company’s products are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearances. The portfolio is listed in the FDA’s 510(k) database, reflecting compliance with U.S. regulatory requirements. The manufacturer operates from the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue6

Newest first, rows 1-6 of 6

Frequently asked questions

How many devices does Woodside Biomedical, Inc. have in the registry?

The registry currently lists 6 devices for Woodside Biomedical, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Woodside Biomedical, Inc.'s devices?

Among its 6 most recently registered devices, Woodside Biomedical, Inc. has devices listed in FDA 510(k) (6 devices).

What risk classes do Woodside Biomedical, Inc.'s devices fall under?

Among its 6 most recently registered devices, the classes recorded for Woodside Biomedical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Woodside Biomedical, Inc. in the registry?

The most recently registered devices listed for Woodside Biomedical, Inc. include RELIEFBAND MST DEVICE, MODELS RB-2, RB-6, RB-R, RELIEFBAND NST DEVICE MODELS WB-2, WB-6, WB-R, RELIEFBAND NST DEVICE, MODEL WB-2L, WB-6L, WB-RL and RELIEFBAND.

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