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Micromri, Inc.

United StatesFDA applicant, unverified

Devices
2

What Micromri, Inc. makes

Micromri, Inc. manufactures the Bonevue imaging agent, a contrast medium used in magnetic resonance imaging (MRI) to enhance visualization of bone structures, and the Micromri Wrist Coil, a specialized MRI coil designed for high-resolution imaging of the wrist.

The company’s portfolio is regulated under FDA Class II devices and is listed via 510(k) premarket notifications. Micromri, Inc. 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

  • Bonevue Ref K083691

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Micromri Wrist Coil Ref K073131

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

Frequently asked questions

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

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

Which registries list Micromri, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Micromri, Inc. include BONEVUE and MICROMRI WRIST COIL.

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