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Emix U.S.A., Inc.

Country not established

Devices
2

What Emix U.S.A., Inc. makes

Emix U.S.A., Inc. manufactures the VELO ACE, a device designed for vascular access and catheterization, and the LUMIX 70B, a contrast agent used in imaging procedures to enhance visibility of blood vessels.

These products are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Velo Ace Ref K940540

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Lumix 70B Ref K951734

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

Frequently asked questions

How many devices does Emix U.S.A., Inc. have in the registry?

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

Which registries list Emix U.S.A., Inc.'s devices?

Among its 2 most recently registered devices, Emix U.S.A., Inc. has devices listed in FDA 510(k) (2 devices).

What risk classes do Emix U.S.A., Inc.'s devices fall under?

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

What are the newest devices from Emix U.S.A., Inc. in the registry?

The most recently registered devices listed for Emix U.S.A., Inc. include VELO ACE and LUMIX 70B.

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