Cg Medtech Co., Ltd.

Cg Medtech Co., Ltd. — FDA 510(k) Submissions

Cg Medtech Co., Ltd. has submitted 2 FDA 510(k) premarket notifications since 2025, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Posterior Cervical Screw System, Intervertebral Fusion Device With Bone Graft, Lumbar . Use the specialty filter in the sidebar to narrow results.