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FDA 510(k)

Endo Motor

K-Number: K192649 · 2021-03-12

ApplicantFoshan Cicada Dental Instrument Co, Ltd.
Decision Date2021-03-12
Product CodeEKX
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Endo Motor is a medical device manufactured by Foshan Cicada Dental Instrument Co, Ltd.. It received FDA 510(k) clearance on 2021-03-12 under approval number K192649. The device is classified under product code EKX. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Endo Motor?

Endo Motor is a medical device that received FDA 510(k) clearance on 2021-03-12. It is manufactured by Foshan Cicada Dental Instrument Co, Ltd.. The 510(k) number is K192649.

When was Endo Motor approved by the FDA?

Endo Motor received FDA 510(k) clearance on 2021-03-12, under approval number K192649.

What company makes Endo Motor?

Endo Motor is manufactured by Foshan Cicada Dental Instrument Co, Ltd..

What is the FDA product code for Endo Motor?

The FDA product code for Endo Motor is EKX.

Other Devices by Foshan Cicada Dental Instrument Co, Ltd.

K181900Dental high speed handpiece, Dental low speed handpiece K192233LED Curing Light K202075Dental Electric Motor

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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.

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