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Rms Div.

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Devices
10

What Rms Div. makes

Rms Div. manufactures radiographic and fluoroscopic imaging equipment, including elevating and tilting radiographic tables (e.g., EXT-600, ELITE 1500, RMS 90/15), spot film devices (e.g., SFD-035), and radiographic spot film drives (e.g., ELITE R/F). Their portfolio also includes medical imaging accessories such as K-wire tools and fiber optic laryngoscopes (e.g., SUNMED'S GREENLINE). Diagnostic X-ray imaging probes (e.g., THE VIVACARE T.P.S. PROBE) and radiographic film devices (e.g., DW250 #91, DW234 #29) are part of their product line.

The company’s devices are classified under FDA’s Class I and Class II categories, with submissions supported by 510(k) clearances. Their products are listed in the FDA’s 510(k) database, reflecting regulatory compliance for medical imaging equipment. Rms Div. is based in the United States.

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

Catalogue10

Newest first, rows 1-10 of 10

  • DW250 #91 Ref K944557

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

  • The Vivacare T.P.S. Probe Ref K944848

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

  • Ext-600 Table, Radiographic, Elevating Ref K896665

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

  • Elite 1500 Radiographic Tilting Table Ref K896324

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

  • Rms 90/15 Radiographic/Fluoroscopic Tilting Table Ref K896119

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

  • Rms K-Wire Ref K963367

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

  • Elite R/F Spot Film Drive Ref K902403

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

  • Sunmed's Greenline Fiber Optic Laryngoscope Ref K954438

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

  • Sfd-035 Spot Film Device Ref K902146

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

  • DW234 #29 Ref K941625

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

Frequently asked questions

How many devices does Rms Div. have in the registry?

The registry currently lists 10 devices for Rms Div.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Rms Div.'s devices?

Among its 10 most recently registered devices, Rms Div. has devices listed in FDA 510(k) (10 devices).

What risk classes do Rms Div.'s devices fall under?

Among its 10 most recently registered devices, the classes recorded for Rms Div.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Rms Div. in the registry?

The most recently registered devices listed for Rms Div. include DW250 #91, THE VIVACARE T.P.S. PROBE, EXT-600 TABLE, RADIOGRAPHIC, ELEVATING and ELITE 1500 RADIOGRAPHIC TILTING TABLE.

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