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Omnicon Medical Corp.

United StatesFDA applicant, unverified

Devices
10

What Omnicon Medical Corp. makes

Omnicon Medical Corp. manufactures disposable and reusable medical devices designed to reduce bacterial contamination in anesthesia and respiratory systems. Their portfolio includes bacteria filters for anesthesia and mainflow circuits, emergency tracheostomy kits, and protective IV line accessories. They also produce conductive anesthesia breathing circuits and Berman airway devices in multiple sizes.

The company’s devices are classified under FDA’s Class I and Class II categories, with regulatory submissions recorded in the FDA’s 510(k) database. Products are listed in the United States, where the manufacturer is based.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue10

Newest first, rows 1-10 of 10

Frequently asked questions

How many devices does Omnicon Medical Corp. have in the registry?

The registry currently lists 10 devices for Omnicon Medical Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Omnicon Medical Corp.'s devices?

Among its 10 most recently registered devices, Omnicon Medical Corp. has devices listed in FDA 510(k) (10 devices).

What risk classes do Omnicon Medical Corp.'s devices fall under?

Among its 10 most recently registered devices, the classes recorded for Omnicon Medical Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Omnicon Medical Corp. in the registry?

The most recently registered devices listed for Omnicon Medical Corp. include ANESTHESIA BACTERIA FILTER, MAINFLOW BACTERIA FILTER, DISPOSABLE BACTERIA FILTER and EMERGENCY TRACHEOSTOMY KIT.

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