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Omnimedical Services, Inc.

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Devices
1

What Omnimedical Services, Inc. makes

Omnimedical Services, Inc. manufactures the OMNIMEDICAL 400L, a medical device designed for large-volume liquid storage and transfer in clinical or procedural settings.

The company’s portfolio is regulated under Class II devices in the United States, with the OMNIMEDICAL 400L listed via FDA 510(k) clearance. The manufacturer is based in the US.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Omnimedical 400l Ref K771990

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

Frequently asked questions

How many devices does Omnimedical Services, Inc. have in the registry?

The registry currently lists 1 device for Omnimedical Services, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Omnimedical Services, Inc.'s devices?

Among its 1 most recently registered device, Omnimedical Services, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Omnimedical Services, Inc.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Omnimedical Services, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Omnimedical Services, Inc. in the registry?

The most recently registered devices listed for Omnimedical Services, Inc. include OMNIMEDICAL 400L.

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