Import Endo Motor — Buy in Bulk from Supplier in China

The Endo motor from Zhengzhou Shengda Dentistry Instrument is a precision electric device designed for endodontic root canal preparation. It features programmable speed and torque settings, allowing clinicians to adjust rotational parameters for different file types and canal anatomies. The unit supports both reciprocating and continuous rotation modes, enabling optimized cutting efficiency while reducing file fracture risk.

The motor is built with a lightweight, ergonomic handpiece interface and a digital display for real-time feedback on RPM and torque output. It includes an apex locator function that can operate independently or simultaneously with the motor function, reducing procedural steps. The device is constructed with medical-grade ABS and stainless steel components, compliant with ISO 13485 for dental instruments. No internal battery is mentioned, suggesting it is designed for wired clinical use only.

This device is used primarily by endodontists and general dentists in private clinics and hospitals requiring reliable, repeatable canal preparation. Buyers include dental distributors in North America, Europe, and Southeast Asia who supply equipment to private practices. Packaging is standard for Class I medical devices: individual box with user manual and power adapter. Trade terms include CIF and L/C. MOQ is flexible but not specified. Lead time and warranty are not stated and must be confirmed with the supplier.

Zhengzhou Shengda Dentistry Instrument is an imported supplier based in Zhengzhou, Henan, China, with a harbor trust tier and no recorded response rate or average response time. The listing provides the supplier's full address but no company history, workforce size, export volume, or client names. It does not claim ownership of a manufacturing facility or R&D department. The supplier is identified solely by name and location.

The supplier's trust tier indicates basic business verification through a harbor platform, confirming registration and physical address. There is no evidence of ISO 13485 certification, clinical testing data, or third-party audits. The CE marking mentioned in the description is claimed but not documented. Buyers must treat this as a trading or OEM supplier, not a certified medical device manufacturer, and verify all technical claims through independent testing.