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Inpharma A.S.

Country not established

Devices
2

What Inpharma A.S. makes

Inpharma A.S. manufactures artificial saliva products, including CAPHOSOL and CAPHOSOL ARTIFICIAL SALIVA, designed to relieve dry mouth symptoms in patients.

These devices are classified as Class II 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.

Catalogue2

Newest first, rows 1-2 of 2

  • Caphosol Artificial Saliva Ref K991938

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

  • Caphosol Ref K030802

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

Frequently asked questions

How many devices does Inpharma A.S. have in the registry?

The registry currently lists 2 devices for Inpharma A.S.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Inpharma A.S.'s devices?

Among its 2 most recently registered devices, Inpharma A.S. has devices listed in FDA 510(k) (2 devices).

What are the newest devices from Inpharma A.S. in the registry?

The most recently registered devices listed for Inpharma A.S. include CAPHOSOL ARTIFICIAL SALIVA and CAPHOSOL.

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