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Nuvue Therapeutics, Inc.

Country not established

Devices
1

What Nuvue Therapeutics, Inc. makes

Nuvue Therapeutics, Inc. manufactures the NUVUE COLORMARK™ needle, a medical device designed for enhanced visibility during procedural use, particularly in subcutaneous or intramuscular injections.

The device is classified as Class II under FDA regulations and is listed in the 510(k) clearance registry. The company 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

  • Nuvue COLORMARK9TM) Needle Ref K101312

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

Frequently asked questions

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

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

Which registries list Nuvue Therapeutics, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Nuvue Therapeutics, Inc. include NUVUE COLORMARK9TM) NEEDLE.

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