Shenzhen Dazhou Medical Technology Co., Ltd.

Shenzhen Dazhou Medical Technology Co., Ltd. — FDA 510(k) Submissions

Shenzhen Dazhou Medical Technology Co., Ltd. has submitted 2 FDA 510(k) premarket notifications since 2024, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Intervertebral Fusion Device With Bone Graft, Lumbar, Bone Grafting Material, Synthetic . Use the specialty filter in the sidebar to narrow results.