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Oxis Intl., Inc.

United StatesFDA 510(k) applicant, unverified

Devices
11

What Oxis Intl., Inc. makes

Oxis Intl., Inc. makes reagent sets and assay systems for various medical tests, including those for theophylline, gentamicin, amikacin, topiramate, phenytoin, phenobarbital, and quinidine. Their products also include discs and control sets for these tests.

The company's portfolio is regulated under Class I and Class II devices and is listed in the FDA 510(k) registry. Oxis Intl., Inc. is based in the US.

AI-generated from registry data, 29 Sep 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

How many devices does Oxis Intl., Inc. have in the registry?

The registry currently lists 11 devices for Oxis Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Oxis Intl., Inc.'s devices?

Among its 11 most recently registered devices, Oxis Intl., Inc. has devices listed in FDA 510(k) (11 devices).

What risk classes do Oxis Intl., Inc.'s devices fall under?

Among its 11 most recently registered devices, the classes recorded for Oxis Intl., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Oxis Intl., Inc. in the registry?

The most recently registered devices listed for Oxis Intl., Inc. include INNOFLOUR TOPIRAMATE REAGENT SET, INNOFLUOR THEOPHYLLINE ASSAY SYSTEM, B-L RED(TM) DISCS and INNOFLUOR GENTAMICIN ASSAY SYSTEM.

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