Manufacturer registered with FDA

Shenzhen Dazhou Medical Technology Co., Ltd.

Shenzhen, China. Lists 2 dental device types with FDA across 1 registered establishment, and holds 1 510(k) clearance as applicant.

FDA owner/operator10090591Manufacturer1 clearance in five years

Device types listed: 2
Brands and models: 3
510(k) clearances: 12025–2025
Markets registered in: 1United States
Establishments: 1China

510(k) clearances per year, 2007–2026

Devices listed with FDA

What Shenzhen Dazhou Medical Technology Co., Ltd. currently lists, by FDA device type, with the brand and model names on the listing.

Device type	Category	Role	Brands and models	Listed since
Intraoral Dental DrillDZA · Class 1	Surgical drills & motors	Maker	Step Drill	2026
Endosseous Dental Implant AccessoriesNDP · Class 1	Implant instruments & surgical kits	Maker	Fixture Mount/TransferRetaining Screw	2026

Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026

510(k) clearances

Clearances on which FDA names Shenzhen Dazhou Medical Technology Co., Ltd. as the applicant.

Decided	510(k)	Device	Device type
21 Feb 2025	K241186	Synthetic Bone Graft Particulate	LYC Synthetic Bone Grafting Material

Registered establishments

Establishment	Location	What it does
SHENZHEN DAZHOU MEDICAL TECHNOLOGY CO., LTD.FDA reg. 3031235905	Shenzhen Guangdong, China	Manufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10090591). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.