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Orison Corporation

United StatesFDA applicant, unverified

Devices
2

What Orison Corporation makes

Orison Corporation makes the Embrace Gel and the Orison Embrace System.

These devices are classified as Class II and are listed in the FDA 510(k) registry; the company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Embrace Gel Ref K072515

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Orison Embrace System Ref K070477

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

Frequently asked questions

How many devices does Orison Corporation have in the registry?

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

Which registries list Orison Corporation's devices?

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

What risk classes do Orison Corporation's devices fall under?

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

What are the newest devices from Orison Corporation in the registry?

The most recently registered devices listed for Orison Corporation include EMBRACE GEL and ORISON EMBRACE SYSTEM.

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