Biodenta Swiss AG

Biodenta Swiss AG manufactures dental implant suprastructures (both permanent and temporary, preformed), surgical drill guides (single-use), two-piece screw endosteal dental implants, dental implant abutment analogs for intraoral scanning (single-use), and dental prosthesis/implant abutment screws. These are the specific device types described in the provided data, and no other products or functions are attributed to the company in this source.

Biodenta Swiss AG is based in Switzerland, as indicated by the country code CH in the device data. This establishes the company’s geographic location without implying any regulatory approval or certification of the company itself.

Devices from Biodenta Swiss AG are listed in Eudamed, the FDA 510(k) database, and the FDA UDI database. These are the only registries explicitly named in the provided data, and listing in these systems reflects device registration, not company approval.

The devices manufactured by Biodenta Swiss AG are classified as Class I, Class II, and Class IIb. This classification reflects the risk-based regulatory categorization of the individual device types, such as surgical drill guides or implant abutments, and does not imply that the company as a whole holds any classification or approval.