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FDA 510(k)

EZ CONNECT

K-Number: K000346 · 2000-04-14

ApplicantKerr Dental Materials Center
Decision Date2000-04-14
Product CodeEBG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

EZ CONNECT is the device name listed in this FDA 510(k) record. The listed applicant is Kerr Dental Materials Center. It received FDA 510(k) clearance on 2000-04-14 under 510(k) number K000346. 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 EZ CONNECT?

EZ CONNECT is a medical device that received FDA 510(k) clearance on 2000-04-14. The listed applicant is Kerr Dental Materials Center. The 510(k) number is K000346.

When did EZ CONNECT receive FDA 510(k) clearance?

EZ CONNECT received FDA 510(k) clearance on 2000-04-14, under 510(k) number K000346.

Who is the listed applicant for EZ CONNECT?

The FDA 510(k) record lists Kerr Dental Materials Center as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EZ CONNECT?

The FDA product code for EZ CONNECT is EBG.

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Other records listing Kerr Dental Materials Center as applicant

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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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