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Yeti Dentalprodukte GmbH

Country not established FDA

Part of Yeti Dentalprodukte GmbH

Devices
340
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA establishment

What Yeti Dentalprodukte GmbH makes

Yeti Dentalprodukte GmbH manufactures dental appliance fabrication materials, specifically ceramic opaquers in powder form. These products are designed for use in dental restorations, including crowns, bridges, and veneers, to enhance opacity and aesthetics in ceramic layers.

The company’s products fall under Class II medical devices and are listed in the FDA’s Unique Device Identifier (UDI) database. The portfolio is regulated under U.S. medical device laws, ensuring compliance with safety and performance standards for dental materials.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue340

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Company details

DUNS number
324001916

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Yeti Dentalprodukte GmbH Engen Baden-Wurttemberg · DE FEI 3006235664

Frequently asked questions

How many devices does Yeti Dentalprodukte GmbH have in the registry?

The registry currently lists 340 devices for Yeti Dentalprodukte GmbH. Devices recorded under merged duplicate company entries are counted once.

Which registries list Yeti Dentalprodukte GmbH's devices?

Among its 50 most recently registered devices, Yeti Dentalprodukte GmbH has devices listed in EUDAMED (30 devices) and FDA GUDID (50 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Yeti Dentalprodukte GmbH's devices fall under?

Among its 50 most recently registered devices, the classes recorded for Yeti Dentalprodukte GmbH's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Yeti Dentalprodukte GmbH in the registry?

The most recently registered devices listed for Yeti Dentalprodukte GmbH include K2 Li-Transpa, T-YE (TRANSPA YELLOW), 20g. 3875004, K2-HF OPAQUER powder, O-A1, 20g. 38620010, K2-HF OPAQUER powder, O-A2, 20g. 3862002 and K2-HF OPAQUER powder, O-A3, 20g. 3862003.

Which FDA establishments are linked to Yeti Dentalprodukte GmbH?

1 FDA establishment is linked to Yeti Dentalprodukte GmbH in the registry; they are listed on the company page.

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