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FDA 510(k)

UNIFAST III

K-Number: K073106 · 2008-04-11

ApplicantGC America, Inc.
Decision Date2008-04-11
Product CodeEBG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

UNIFAST III is the device name listed in this FDA 510(k) record. The listed applicant is GC America, Inc.. It received FDA 510(k) clearance on 2008-04-11 under 510(k) number K073106. 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 UNIFAST III?

UNIFAST III is a medical device that received FDA 510(k) clearance on 2008-04-11. The listed applicant is GC America, Inc.. The 510(k) number is K073106.

When did UNIFAST III receive FDA 510(k) clearance?

UNIFAST III received FDA 510(k) clearance on 2008-04-11, under 510(k) number K073106.

Who is the listed applicant for UNIFAST III?

The FDA 510(k) record lists GC America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UNIFAST III?

The FDA product code for UNIFAST III is EBG.

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Other records listing GC America, Inc. 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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