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FDA 510(k)

INTERIM TEMP. CROWN & BRIDGE RESIN

K-Number: K833261 · 1984-01-03

ApplicantCoe Laboratories, Inc.
Decision Date1984-01-03
Product CodeEBG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

INTERIM TEMP. CROWN & BRIDGE RESIN is the device name listed in this FDA 510(k) record. The listed applicant is Coe Laboratories, Inc.. It received FDA 510(k) clearance on 1984-01-03 under 510(k) number K833261. 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 INTERIM TEMP. CROWN & BRIDGE RESIN?

INTERIM TEMP. CROWN & BRIDGE RESIN is a medical device that received FDA 510(k) clearance on 1984-01-03. The listed applicant is Coe Laboratories, Inc.. The 510(k) number is K833261.

When did INTERIM TEMP. CROWN & BRIDGE RESIN receive FDA 510(k) clearance?

INTERIM TEMP. CROWN & BRIDGE RESIN received FDA 510(k) clearance on 1984-01-03, under 510(k) number K833261.

Who is the listed applicant for INTERIM TEMP. CROWN & BRIDGE RESIN?

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

What is the FDA product code for INTERIM TEMP. CROWN & BRIDGE RESIN?

The FDA product code for INTERIM TEMP. CROWN & BRIDGE RESIN is EBG.

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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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