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FDA 510(k)

EzDent Web

K-Number: K230468 · 2023-04-21

ApplicantEwoosoft Co., Ltd.
Decision Date2023-04-21
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

EzDent Web is a medical device manufactured by Ewoosoft Co., Ltd.. It received FDA 510(k) clearance on 2023-04-21 under approval number K230468. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EzDent Web?

EzDent Web is a medical device that received FDA 510(k) clearance on 2023-04-21. It is manufactured by Ewoosoft Co., Ltd.. The 510(k) number is K230468.

When was EzDent Web approved by the FDA?

EzDent Web received FDA 510(k) clearance on 2023-04-21, under approval number K230468.

What company makes EzDent Web?

EzDent Web is manufactured by Ewoosoft Co., Ltd..

What is the FDA product code for EzDent Web?

The FDA product code for EzDent Web is LLZ.

Other Devices by Ewoosoft Co., Ltd.

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Related Devices (Code: LLZ)

K161959ClearView cCADClearview Diagnostics, Inc. K163539Ez3D-i / E3Ewoosoft Co., Ltd. K162955Multi-Modality Tumor Tracking (MMTT) applicationPhilips Medical Systems Nederland B.V. K160852ZiaZetta Medical Technologies, LLC K162376CAAS MR 4D FlowPie Medical Imaging BV K161322CT CoPilotZepmed, LLC

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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