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Rota Systems Medfurniture, Inc.

United StatesFDA applicant, unverified

Devices
2

What Rota Systems Medfurniture, Inc. makes

Rota Systems Medfurniture, Inc. manufactures mobile medical furniture systems, including the ROTA SYSTEM XL and ROTA SYSTEM 5000, designed for hospital and clinical environments. These products provide modular, adjustable storage and work surfaces for medical supplies, equipment, and patient care items. The systems are engineered to enhance workflow efficiency and space utilization in healthcare settings.

The company’s products are classified as Class I medical devices under FDA regulations and are supported by 510(k) clearance records. The portfolio is listed in the FDA’s 510(k) database, reflecting compliance with U.S. device authorization requirements. The manufacturer operates from 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

  • Rota System Xl Ref K931839

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Rota System 5000 Ref K935952

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

Frequently asked questions

How many devices does Rota Systems Medfurniture, Inc. have in the registry?

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

Which registries list Rota Systems Medfurniture, Inc.'s devices?

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

What risk classes do Rota Systems Medfurniture, Inc.'s devices fall under?

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

What are the newest devices from Rota Systems Medfurniture, Inc. in the registry?

The most recently registered devices listed for Rota Systems Medfurniture, Inc. include ROTA SYSTEM XL and ROTA SYSTEM 5000.

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