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Oraltronics Dental Implant Technology GmbH

Country not established

Devices
1

What Oraltronics Dental Implant Technology GmbH makes

Oraltronics Dental Implant Technology GmbH manufactures the BIORESORB MACRO PORE, a resorbable implant material designed for dental applications, intended to support bone regeneration and integration in oral surgery procedures.

The company’s portfolio is regulated under FDA 510(k) clearance as a Class II medical device and is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Bioresorb Macro Pore Ref K050260

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

Frequently asked questions

How many devices does Oraltronics Dental Implant Technology GmbH have in the registry?

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

Which registries list Oraltronics Dental Implant Technology GmbH's devices?

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

What risk classes do Oraltronics Dental Implant Technology GmbH's devices fall under?

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

What are the newest devices from Oraltronics Dental Implant Technology GmbH in the registry?

The most recently registered devices listed for Oraltronics Dental Implant Technology GmbH include BIORESORB MACRO PORE.

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