Proimtech Saglik Urunleri Anonim Sirketi

Proimtech Saglik Urunleri Anonim Sirketi — FDA 510(k) Submissions

Proimtech Saglik Urunleri Anonim Sirketi has submitted 3 FDA 510(k) premarket notifications since 2024, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Implant, Endosseous, Orthodontic, Screw, Fixation, Intraosseous, Implant, Endosseous, Root-form . Use the specialty filter in the sidebar to narrow results.