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Medicom Group, Inc.

CanadaFDA applicant, unverified

Devices
1

What Medicom Group, Inc. makes

Medicom Group, Inc. manufactures Medicom Sterilization Wrap, a barrier material designed for use in medical sterilization processes to protect packaged devices from contamination during autoclaving or ethylene oxide sterilization.

The company’s product portfolio is regulated under FDA Class II devices and is listed via 510(k) clearance. The manufacturer is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Medicom Sterilization Wrap Ref K240862

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

Frequently asked questions

How many devices does Medicom Group, Inc. have in the registry?

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

Which registries list Medicom Group, Inc.'s devices?

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

What risk classes do Medicom Group, Inc.'s devices fall under?

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

What are the newest devices from Medicom Group, Inc. in the registry?

The most recently registered devices listed for Medicom Group, Inc. include Medicom Sterilization Wrap.

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