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Phasealloy

Country not established

Devices
2

What Phasealloy makes

Phasealloy manufactures medical devices for vascular access, including a powered injection system for contrast media and a disposable infusion set designed for intravenous procedures.

The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) pathway. Phasealloy is based in the United States.

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

Catalogue2

Newest first, rows 1-2 of 2

  • Phaseafill Ref K782165

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • First Tm Ref K830513

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

Frequently asked questions

How many devices does Phasealloy have in the registry?

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

Which registries list Phasealloy's devices?

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

What risk classes do Phasealloy's devices fall under?

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

What are the newest devices from Phasealloy in the registry?

The most recently registered devices listed for Phasealloy include PHASEAFILL and FIRST TM.

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