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FDA 510(k)

INSURE MATCH MATE PORCELAIN VENEER TRY-IN SYSTEM

K-Number: K894477 · 1990-01-10

Decision Date1990-01-10
Product CodeEMA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

INSURE MATCH MATE PORCELAIN VENEER TRY-IN SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Cosmedent, Inc.. It received FDA 510(k) clearance on 1990-01-10 under 510(k) number K894477. The device is classified under product code EMA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSURE MATCH MATE PORCELAIN VENEER TRY-IN SYSTEM?

INSURE MATCH MATE PORCELAIN VENEER TRY-IN SYSTEM is a medical device that received FDA 510(k) clearance on 1990-01-10. The listed applicant is Cosmedent, Inc.. The 510(k) number is K894477.

When did INSURE MATCH MATE PORCELAIN VENEER TRY-IN SYSTEM receive FDA 510(k) clearance?

INSURE MATCH MATE PORCELAIN VENEER TRY-IN SYSTEM received FDA 510(k) clearance on 1990-01-10, under 510(k) number K894477.

Who is the listed applicant for INSURE MATCH MATE PORCELAIN VENEER TRY-IN SYSTEM?

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

What is the FDA product code for INSURE MATCH MATE PORCELAIN VENEER TRY-IN SYSTEM?

The FDA product code for INSURE MATCH MATE PORCELAIN VENEER TRY-IN SYSTEM is EMA.

Related Clinical Trials

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.

Other records listing Cosmedent, 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.

View all 28 devices →

Related Devices (Code: EMA)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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