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Shenzhen Dazhou Medical Technology Co., Ltd.

ChinaFDA applicant, unverified FDA FEI 3031235905

Devices
2
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

What Shenzhen Dazhou Medical Technology Co., Ltd. makes

Shenzhen Dazhou Medical Technology Co., Ltd. manufactures spinal implants, including the DZ-Tabone Intervertebral Body Fusion Device for surgical fusion of vertebrae, and synthetic bone graft particulate for use in bone regeneration procedures.

Their devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company operates from the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

Company details

FDA FEI number
3031235905
Address
Suite B605, Building No.1, YESUN INTELLIGENT COMMUNITY II, 1301-76 Guanguang Rd., Longhua District, Shenzhen Guangdong

Frequently asked questions

How many devices does Shenzhen Dazhou Medical Technology Co., Ltd. have in the registry?

The registry currently lists 2 devices for Shenzhen Dazhou Medical Technology Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Shenzhen Dazhou Medical Technology Co., Ltd.'s devices?

Among its 2 most recently registered devices, Shenzhen Dazhou Medical Technology Co., Ltd. has devices listed in FDA 510(k) (2 devices).

What risk classes do Shenzhen Dazhou Medical Technology Co., Ltd.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Shenzhen Dazhou Medical Technology Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Shenzhen Dazhou Medical Technology Co., Ltd. in the registry?

The most recently registered devices listed for Shenzhen Dazhou Medical Technology Co., Ltd. include DZ-Tabone Intervertebral Body Fusion Device and Synthetic Bone Graft Particulate.

Generated automatically from registry data and not verified by a human reviewer.