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Halmon-Locren, Inc.

Country not established

Devices
1

What Halmon-Locren, Inc. makes

Halmon-Locren, Inc. manufactures the ARISTOSURG 250, a surgical device designed for precise tissue manipulation during medical procedures.

The ARISTOSURG 250 is classified as a Class I medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Aristosurg 250 Ref K800395

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

Frequently asked questions

How many devices does Halmon-Locren, Inc. have in the registry?

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

Which registries list Halmon-Locren, Inc.'s devices?

Among its 1 most recently registered device, Halmon-Locren, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Halmon-Locren, Inc.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Halmon-Locren, Inc.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Halmon-Locren, Inc. in the registry?

The most recently registered devices listed for Halmon-Locren, Inc. include ARISTOSURG 250.

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