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Onepacs, LLC

United Statesfrom the FDA registration address FDA FEI 3030228575

Devices
1
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

What Onepacs, LLC makes

Onepacs, LLC produces the OnePacs System, which is a medical imaging software platform.

The device is classified as Class II and is listed in the FDA 510(k) database, with the company based in the United States.

AI-generated from registry data, 5 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • OnePacs System Ref K181460

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

Company details

FDA FEI number
3030228575
Address
8777 Velocity Drive, Machesney Park, IL, 61115

Frequently asked questions

How many devices does Onepacs, LLC have in the registry?

The registry currently lists 1 device for Onepacs, LLC. Devices recorded under merged duplicate company entries are counted once.

Which registries list Onepacs, LLC's devices?

Among its 1 most recently registered device, Onepacs, LLC has devices listed in FDA 510(k) (1 device).

What risk classes do Onepacs, LLC's devices fall under?

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

What are the newest devices from Onepacs, LLC in the registry?

The most recently registered devices listed for Onepacs, LLC include OnePacs System.

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