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FDA 510(k)

EzDent-i / E2 / Prora View/ Smart M Viewer

K-Number: K223820 · 2023-02-17

ApplicantEwoosoft Co., Ltd.
Decision Date2023-02-17
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

EzDent-i / E2 / Prora View/ Smart M Viewer is the device name listed in this FDA 510(k) record. The listed applicant is Ewoosoft Co., Ltd.. It received FDA 510(k) clearance on 2023-02-17 under 510(k) number K223820. 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?

EzDent-i / E2 / Prora View/ Smart M Viewer is a medical device that received FDA 510(k) clearance on 2023-02-17. The listed applicant is Ewoosoft Co., Ltd.. The 510(k) number is K223820.

When did EzDent-i / E2 / Prora View/ Smart M Viewer receive FDA 510(k) clearance?

EzDent-i / E2 / Prora View/ Smart M Viewer received FDA 510(k) clearance on 2023-02-17, under 510(k) number K223820.

Who is the listed applicant for EzDent-i / E2 / Prora View/ Smart M Viewer?

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

What is the FDA product code for EzDent-i / E2 / Prora View/ Smart M Viewer?

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

Other records listing Ewoosoft Co., Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K250005Clever OneK241114EzDent-i / E2 / Prora View / Smart M Viewer (v3.5)K231757Ez3D-i /E3K230468EzDent WebK222069Ez3D-i/E3K222145EzDent-i / E2 / Prora View/ Smart M Viewer

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Related Devices (Code: LLZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K262449AdvaViewADVAHEALTH SOLUTIONS, LLCK261916NeuroQuant PETCortechs Labs, Inc.K260936RadioViewAINeurocareai, Inc. (Dba Savelife.Ai)K260588Cleerly LABSCleerly, Inc.K262462TheraSphere 360™ Y-90 Management PlatformBoston Scientific CorporationK262143ImageGrid StreamVueCandelis, 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.

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