Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Dental High-speed Turbine Handpiece

K-Number: K170229 · 2017-11-08

Decision Date2017-11-08
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Dental High-speed Turbine Handpiece is a medical device manufactured by Guangdong Jinme Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2017-11-08 under approval number K170229. 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 High-speed Turbine Handpiece?

Dental High-speed Turbine Handpiece is a medical device that received FDA 510(k) clearance on 2017-11-08. It is manufactured by Guangdong Jinme Medical Technology Co., Ltd.. The 510(k) number is K170229.

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

Dental High-speed Turbine Handpiece received FDA 510(k) clearance on 2017-11-08, under approval number K170229.

What company makes Dental High-speed Turbine Handpiece?

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

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

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

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

Related Devices (Code: EFB)

Official Source

View on FDA Database →

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