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Schuetz Dental GmbH

GermanyFDA applicant, unverified

Devices
1

What Schuetz Dental GmbH makes

Schuetz Dental GmbH manufactures dental bulk-fill restorative materials, including the CAPO BULK FILL composite resin, designed for efficient layering in posterior restorations.

The company’s portfolio is regulated under FDA Class II devices, with products listed via the 510(k) clearance pathway. The manufacturer is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Capo Bulk Fill Ref K152471

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

Company details

Other identifier
7300(not a standard FEI format)
Address
DIESELSTRASSE 5-6, ROSBACH Hesse

Frequently asked questions

How many devices does Schuetz Dental GmbH have in the registry?

The registry currently lists 1 device for Schuetz Dental GmbH. Devices recorded under merged duplicate company entries are counted once.

Which registries list Schuetz Dental GmbH's devices?

Among its 1 most recently registered device, Schuetz Dental GmbH has devices listed in FDA 510(k) (1 device).

What risk classes do Schuetz Dental GmbH's devices fall under?

Among its 1 most recently registered device, the classes recorded for Schuetz Dental GmbH's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Schuetz Dental GmbH in the registry?

The most recently registered devices listed for Schuetz Dental GmbH include CAPO BULK FILL.

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