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FDA 510(k)

EzDent-i / E2 / Prora View / Smart M Viewer (v3.5)

K-Number: K241114 · 2024-07-23

Decision Date2024-07-23
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

EzDent-i / E2 / Prora View / Smart M Viewer (v3.5) is a medical device manufactured by Ewoosoft Co., Ltd.. It received FDA 510(k) clearance on 2024-07-23 under approval number K241114. 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-i / E2 / Prora View / Smart M Viewer (v3.5)?

EzDent-i / E2 / Prora View / Smart M Viewer (v3.5) is a medical device that received FDA 510(k) clearance on 2024-07-23. It is manufactured by Ewoosoft Co., Ltd.. The 510(k) number is K241114.

When was EzDent-i / E2 / Prora View / Smart M Viewer (v3.5) approved by the FDA?

EzDent-i / E2 / Prora View / Smart M Viewer (v3.5) received FDA 510(k) clearance on 2024-07-23, under approval number K241114.

What company makes EzDent-i / E2 / Prora View / Smart M Viewer (v3.5)?

EzDent-i / E2 / Prora View / Smart M Viewer (v3.5) is manufactured by Ewoosoft Co., Ltd..

What is the FDA product code for EzDent-i / E2 / Prora View / Smart M Viewer (v3.5)?

The FDA product code for EzDent-i / E2 / Prora View / Smart M Viewer (v3.5) is LLZ.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.