Micro-Nx Co., Ltd.

Micro-Nx Co., Ltd. — FDA 510(k) Submissions

Micro-Nx Co., Ltd. has submitted 7 FDA 510(k) premarket notifications since 2017, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Controller, Foot, Handpiece And Cord, Handpiece, Direct Drive, Ac-powered, Handpiece, Belt And/or Gear Driven, Dental, Handpiece, Contra- And Right-angle Attachment, Dental . Use the specialty filter in the sidebar to narrow results.