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Quantum Devices, Inc.

United StatesFDA applicant, unverified

Devices
2

What Quantum Devices, Inc. makes

Quantum Devices, Inc. manufactures light delivery systems, including the Quantum Warp 10 and variants such as the WARP10 and WARP75, designed for controlled illumination in medical applications.

These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Quantum Warp 10 Light Delivery System Ref K032229

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • WARP10, WARP75 Ref K113231

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

Frequently asked questions

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

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

Which registries list Quantum Devices, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Quantum Devices, Inc. include QUANTUM WARP 10 LIGHT DELIVERY SYSTEM and WARP10, WARP75.

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