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Midwest

Country not established

Devices
13

What Midwest makes

Midwest manufactures dental handpieces and optical systems, including high-speed turbine handpieces, fiber optic attachments, and air motor-driven tools for precision dental procedures. Their portfolio includes straight and contra-angle attachments, light sources for fiber optics, and dental hoses with integrated light conductors. Additional products feature integrated lighting for internal dental applications and power optics for enhanced visibility during treatments.

The company’s devices are classified under FDA’s Class I and Class II categories, with most requiring 510(k) clearance. Their products are listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue13

Newest first, rows 1-13 of 13

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  • Ls-100 Ref K792302

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

  • Mw Straight Attachment Ref K792445

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

  • Am-40 Power Optic Air Motor Power Optic Contra Ang Ref K850344

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

  • Light-Pak Ref K791733

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

  • Mw-8000 Ref K792304

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

  • Mw 8000-I Ref K792303

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

  • Fiber Optics High Speed Handpiece Ref K760794

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

  • Tradition High Speed Handpiece Ref K863677

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

  • Oraluminator Iii - Light Source For F.O. Ref K760796

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

  • Fiber Optics Dental Hose W/Integral L.C. Ref K760795

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

  • Oraluminator Iii Auto-Light Ref K791771

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

  • Light, Inside Ref K781878

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

  • Midwest 1000 Ref K790113

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

Rows 1-13 of 13

Frequently asked questions

How many devices does Midwest have in the registry?

The registry currently lists 13 devices for Midwest. Devices recorded under merged duplicate company entries are counted once.

Which registries list Midwest's devices?

Among its 13 most recently registered devices, Midwest has devices listed in FDA 510(k) (13 devices).

What risk classes do Midwest's devices fall under?

Among its 13 most recently registered devices, the classes recorded for Midwest's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Midwest in the registry?

The most recently registered devices listed for Midwest include LS-100, MW STRAIGHT ATTACHMENT, AM-40 POWER OPTIC AIR MOTOR POWER OPTIC CONTRA ANG and LIGHT-PAK.

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