Izenimplant Co., Ltd.

Izenimplant Co., Ltd. — FDA 510(k) Submissions

Izenimplant Co., Ltd. has submitted 7 FDA 510(k) premarket notifications since 2022, of which 7 received clearance as substantially equivalent to a predicate device.

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