Skip to content

Roman Laboratories, Inc.

United StatesFDA applicant, unverified

Devices
2

What Roman Laboratories, Inc. makes

Roman Laboratories, Inc. manufactures the MOBIL 02 and MOBIL-AIR, which are mobility assistance devices designed for patient transfer and positioning in clinical settings.

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

  • Mobil 02 Ref K864680

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Mobil-Air Ref K870064

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

Frequently asked questions

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

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

Which registries list Roman Laboratories, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Roman Laboratories, Inc. include MOBIL 02 and MOBIL-AIR.

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