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Robert W. Bauer & Assoc., Inc.

United StatesFDA applicant, unverified

Devices
3

What Robert W. Bauer & Assoc., Inc. makes

Robert W. Bauer & Assoc., Inc. manufactures dental impression materials, including ALGIDENCO and ALGIPRINT, used for creating precise molds of oral structures. The company also produces the COMPA LAB-R, a laboratory device for processing dental impressions, and the ORAL STEEL cartridge syringe, designed for dispensing dental materials.

These products are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearance records. The company operates from the United States.

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

Catalogue3

Newest first, rows 1-3 of 3

  • Algidenco And Algiprint Impression Materials Ref K942219

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Compa Lab-R Ref K950765

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Oral Steel Cartridge Syringe Ref K941915

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

Frequently asked questions

How many devices does Robert W. Bauer & Assoc., Inc. have in the registry?

The registry currently lists 3 devices for Robert W. Bauer & Assoc., Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Robert W. Bauer & Assoc., Inc.'s devices?

Among its 3 most recently registered devices, Robert W. Bauer & Assoc., Inc. has devices listed in FDA 510(k) (3 devices).

What risk classes do Robert W. Bauer & Assoc., Inc.'s devices fall under?

Among its 3 most recently registered devices, the classes recorded for Robert W. Bauer & Assoc., Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Robert W. Bauer & Assoc., Inc. in the registry?

The most recently registered devices listed for Robert W. Bauer & Assoc., Inc. include ALGIDENCO AND ALGIPRINT IMPRESSION MATERIALS, COMPA LAB-R and ORAL STEEL CARTRIDGE SYRINGE.

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