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)

Endo Motor

K-Number: K222548 · 2023-04-26

ApplicantShenzhen Perfect Medical Instruments Co., Ltd.
Decision Date2023-04-26
Product CodeEKX
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Endo Motor is a medical device manufactured by Shenzhen Perfect Medical Instruments Co., Ltd.. It received FDA 510(k) clearance on 2023-04-26 under approval number K222548. 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 2023-04-26. It is manufactured by Shenzhen Perfect Medical Instruments Co., Ltd.. The 510(k) number is K222548.

When was Endo Motor approved by the FDA?

Endo Motor received FDA 510(k) clearance on 2023-04-26, under approval number K222548.

What company makes Endo Motor?

Endo Motor is manufactured by Shenzhen Perfect Medical Instruments Co., Ltd..

What is the FDA product code for Endo Motor?

The FDA product code for Endo Motor is EKX.

Related Devices (Code: EKX)

K160825MIDWEST RDH Freedom Cordless Prophy System with SmartMode TechnologyDentsply Sirona K153285EMS-200Meta Systems Co., Ltd. K143445Tellos ISQ BuddyTellos Medical AB K170275Tri Auto ZX2J. Morita USA, Inc. K161500MEG-TORQMicro-Nx Co., Ltd. K173920LS OILJ. Morita USA, Inc.

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.

↑