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Phantom Technologies, Inc.

United StatesFDA applicant, unverified

Devices
2

What Phantom Technologies, Inc. makes

Phantom Technologies, Inc. manufactures the SCANTECH Laser Scanner, a device used for precise optical scanning applications, and the ErBIUM 2000 Laser Family, a series of erbium-doped laser systems designed for medical procedures.

These products are classified as Class II devices under FDA regulations and are listed via the 510(k) clearance process. 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

  • Scantech Laser Scanner Ref K974633

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Erbium 2000 Laser Family Ref K972915

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

Frequently asked questions

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

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

Which registries list Phantom Technologies, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Phantom Technologies, Inc. include SCANTECH LASER SCANNER and ERBIUM 2000 LASER FAMILY.

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