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Duncan Hynd Associates, Ltd.

Country not established

Devices
2

What Duncan Hynd Associates, Ltd. makes

Duncan Hynd Associates, Ltd. manufactures the INVAC, a device designed for invasive monitoring applications, and the PROFA, a product intended for professional use in medical diagnostics or treatment procedures.

The company’s portfolio is regulated under FDA Class II devices, with products listed via the 510(k) clearance pathway. The manufacturer 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

  • Invac Ref K002608

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

  • Profa Ref K981911

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

Frequently asked questions

How many devices does Duncan Hynd Associates, Ltd. have in the registry?

The registry currently lists 2 devices for Duncan Hynd Associates, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Duncan Hynd Associates, Ltd.'s devices?

Among its 2 most recently registered devices, Duncan Hynd Associates, Ltd. has devices listed in FDA 510(k) (2 devices).

What risk classes do Duncan Hynd Associates, Ltd.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Duncan Hynd Associates, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Duncan Hynd Associates, Ltd. in the registry?

The most recently registered devices listed for Duncan Hynd Associates, Ltd. include INVAC and PROFA.

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