Friatec AG - FDA 510(k) Cleared Devices

Friatec AG, is a dental device manufacturer with a manufacturing facility in Potomac, US. The company specializes in dental implant systems and related surgical components.

Friatec AG received 6 FDA 510(k) clearances from 6 total submissions, all within the dental device category. The company's regulatory activity spans from 1998 to 1998. This represents a historical record; the company has not submitted new clearances in more than five years and is considered inactive.

The company's cleared portfolio includes implant abutments, cylinders, screws, and bone grafting materials. These products reflect core competencies in osseointegrated implant technology and surgical restoration systems for dental applications.

Review the complete list of device names, model numbers, and clearance dates in the database to explore Friatec AG's regulatory history.