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FDA 510(k)

Ez3D-i /E3

K-Number: K231757 · 2023-07-14

ApplicantEwoosoft Co., Ltd.
Decision Date2023-07-14
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Ez3D-i /E3 is a medical device manufactured by Ewoosoft Co., Ltd.. It received FDA 510(k) clearance on 2023-07-14 under approval number K231757. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Ez3D-i /E3?

Ez3D-i /E3 is a medical device that received FDA 510(k) clearance on 2023-07-14. It is manufactured by Ewoosoft Co., Ltd.. The 510(k) number is K231757.

When was Ez3D-i /E3 approved by the FDA?

Ez3D-i /E3 received FDA 510(k) clearance on 2023-07-14, under approval number K231757.

What company makes Ez3D-i /E3?

Ez3D-i /E3 is manufactured by Ewoosoft Co., Ltd..

What is the FDA product code for Ez3D-i /E3?

The FDA product code for Ez3D-i /E3 is QIH.

Other Devices by Ewoosoft Co., Ltd.

K163539Ez3D-i / E3 K161246Ez3D-i / E3 K161117EzDent-i / E2 / Prora View K152746Ez3D Plus K173094OrthoVision K172364EzDent-i / E2 / Prora View

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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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