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FDA 510(k)

Endo Motor

K-Number: K220829 · 2023-05-18

ApplicantFoshan Coxo Medical Instrument Co., Ltd.
Decision Date2023-05-18
Product CodeEKX
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Endo Motor is the device name listed in this FDA 510(k) record. The listed applicant is Foshan Coxo Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2023-05-18 under 510(k) number K220829. 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 2023-05-18. The listed applicant is Foshan Coxo Medical Instrument Co., Ltd.. The 510(k) number is K220829.

When did Endo Motor receive FDA 510(k) clearance?

Endo Motor received FDA 510(k) clearance on 2023-05-18, under 510(k) number K220829.

Who is the listed applicant for Endo Motor?

The FDA 510(k) record lists Foshan Coxo Medical Instrument Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Endo Motor?

The FDA product code for Endo Motor is EKX.

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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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