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Izun Pharmaceuticals Corporation

Also registered as Izun Pharmaceuticals

United StatesFDA applicant, unverified

Devices
2

What Izun Pharmaceuticals Corporation makes

Izun Pharmaceuticals Corporation manufactures the PerioPatch, which is a medical device designed for oral applications.

This device is regulated under the FDA 510(k) pathway and is listed in the FDA 510(k) registry, with the company based in the United States.

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

Catalogue2

Newest first, rows 1-2 of 2

  • Curasite Ref K161991

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

  • Periopatch Ref K103054

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

Frequently asked questions

How many devices does Izun Pharmaceuticals Corporation have in the registry?

The registry currently lists 2 devices for Izun Pharmaceuticals Corporation. Devices recorded under merged duplicate company entries are counted once.

Which registries list Izun Pharmaceuticals Corporation's devices?

Among its 2 most recently registered devices, Izun Pharmaceuticals Corporation has devices listed in FDA 510(k) (2 devices).

What are the newest devices from Izun Pharmaceuticals Corporation in the registry?

The most recently registered devices listed for Izun Pharmaceuticals Corporation include Curasite and PERIOPATCH.

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