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S.H.P. Intl. Pty., Ltd.

Country not established

Devices
2

What S.H.P. Intl. Pty., Ltd. makes

S.H.P. Intl. Pty., Ltd. manufactures the ACUPLUS, a medical device designed for surgical applications, and the ACUSTIM, a device used for acoustic stimulation or therapy. These products serve distinct clinical purposes within their respective categories, focusing on precision and procedural support.

The company’s portfolio includes Class II and Unclassified (U) devices, with regulatory authorisation through FDA 510(k) clearance. These devices are listed under U.S. regulatory frameworks, and the manufacturer operates from 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

  • Acuplus Ref K954334

    Class II
    Active 510(k) 510(k) II

  • Acustim Ref K014273

    Unclassified
    Active 510(k) 510(k) —

Frequently asked questions

How many devices does S.H.P. Intl. Pty., Ltd. have in the registry?

The registry currently lists 2 devices for S.H.P. Intl. Pty., Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list S.H.P. Intl. Pty., Ltd.'s devices?

Among its 2 most recently registered devices, S.H.P. Intl. Pty., Ltd. has devices listed in FDA 510(k) (2 devices).

What risk classes do S.H.P. Intl. Pty., Ltd.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for S.H.P. Intl. Pty., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from S.H.P. Intl. Pty., Ltd. in the registry?

The most recently registered devices listed for S.H.P. Intl. Pty., Ltd. include ACUPLUS and ACUSTIM.

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