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FDA 510(k)

Dental Low-speed Turbine Handpiece

K-Number: K170236 · 2017-11-21

Decision Date2017-11-21
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Dental Low-speed Turbine Handpiece is a medical device manufactured by Guangdong Jinme Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2017-11-21 under approval number K170236. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Dental Low-speed Turbine Handpiece?

Dental Low-speed Turbine Handpiece is a medical device that received FDA 510(k) clearance on 2017-11-21. It is manufactured by Guangdong Jinme Medical Technology Co., Ltd.. The 510(k) number is K170236.

When was Dental Low-speed Turbine Handpiece approved by the FDA?

Dental Low-speed Turbine Handpiece received FDA 510(k) clearance on 2017-11-21, under approval number K170236.

What company makes Dental Low-speed Turbine Handpiece?

Dental Low-speed Turbine Handpiece is manufactured by Guangdong Jinme Medical Technology Co., Ltd..

What is the FDA product code for Dental Low-speed Turbine Handpiece?

The FDA product code for Dental Low-speed Turbine Handpiece is EFB.

Other Devices by Guangdong Jinme Medical Technology Co., Ltd.

Related Devices (Code: EFB)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.