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Midwest Dental Products Corp.

United StatesFDA applicant, unverified

Devices
5

What Midwest Dental Products Corp. makes

Midwest Dental Products Corp. manufactures dental equipment including the Microjet cavity preparation system, the Midwest 300 SE, Midwest One, 23:1 reduction angle, and the Tradition P push button handpiece.

The company is based in the United States, and its portfolio consists of Class I and Class II medical devices that are listed in the FDA 510(k) registry.

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

Catalogue5

Newest first, rows 1-5 of 5

  • Microjet Cavity Preparation System Ref K964755

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Midwest 300 Se Ref K962877

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Midwest One Ref K955655

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • 23:1 Reduction Angle Ref K973800

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Tradition P, Push Button Handpiece Ref K963050

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

Frequently asked questions

How many devices does Midwest Dental Products Corp. have in the registry?

The registry currently lists 5 devices for Midwest Dental Products Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Midwest Dental Products Corp.'s devices?

Among its 5 most recently registered devices, Midwest Dental Products Corp. has devices listed in FDA 510(k) (5 devices).

What risk classes do Midwest Dental Products Corp.'s devices fall under?

Among its 5 most recently registered devices, the classes recorded for Midwest Dental Products Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Midwest Dental Products Corp. in the registry?

The most recently registered devices listed for Midwest Dental Products Corp. include MICROJET CAVITY PREPARATION SYSTEM, MIDWEST 300 SE, MIDWEST ONE and 23:1 REDUCTION ANGLE.

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