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North, Inc.

United StatesFDA applicant, unverified

Devices
2

What North, Inc. makes

North, Inc. manufactures medical devices including the TRI-FLOW THREE WAY STOPCOCK and the EASI-JECTOR CONTROL SYSTEM.

These devices are Class II and listed in the FDA 510(k) registry. The company is based in the US.

AI-generated from registry data, 30 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Tri-Flow Three Way Stopcock Ref K961982

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Easi-Jector Control System Ref K954189

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

Frequently asked questions

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

The registry currently lists 2 devices for North, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list North, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for North, Inc. include TRI-FLOW THREE WAY STOPCOCK and EASI-JECTOR CONTROL SYSTEM.

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