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FDA 510(k)

Structur CAD

K-Number: K201090 · 2020-09-09

ApplicantVoco GmbH
Decision Date2020-09-09
Product CodeEBG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Structur CAD is the device name listed in this FDA 510(k) record. The listed applicant is Voco GmbH. It received FDA 510(k) clearance on 2020-09-09 under 510(k) number K201090. The device is classified under product code EBG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Structur CAD?

Structur CAD is a medical device that received FDA 510(k) clearance on 2020-09-09. The listed applicant is Voco GmbH. The 510(k) number is K201090.

When did Structur CAD receive FDA 510(k) clearance?

Structur CAD received FDA 510(k) clearance on 2020-09-09, under 510(k) number K201090.

Who is the listed applicant for Structur CAD?

The FDA 510(k) record lists Voco GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Structur CAD?

The FDA product code for Structur CAD is EBG.

Other records listing Voco GmbH 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.

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Related Devices (Code: EBG)

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.

K261261Dura-ArchHangzhou SHINING3D Dental Technology Co., Ltd.K253380“FLNT Base” and “FLNT Temp”Liaoning Upcera Co., Ltd.K251271TempFIT Temporary Crown and Bridge ResinRizhao Huge Biomaterials Company, Ltd.K243370DentaTOOTHAsiga Pty, Ltd.K243621Evoblock, PerléonEvoden Indústria Comércio Importação E ExportaçãoK243951TEMP MASTER, PMMA-based dental resinTaiwan Dental Materials Co., Ltd.

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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