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FDA 510(k)

MULTIPLE (TOOTH DESENSITIZER)

K-Number: K052263 · 2005-12-16

ApplicantCosmedent, Inc.
Decision Date2005-12-16
Product CodeLBH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MULTIPLE (TOOTH DESENSITIZER) is the device name listed in this FDA 510(k) record. The listed applicant is Cosmedent, Inc.. It received FDA 510(k) clearance on 2005-12-16 under 510(k) number K052263. The device is classified under product code LBH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTIPLE (TOOTH DESENSITIZER)?

MULTIPLE (TOOTH DESENSITIZER) is a medical device that received FDA 510(k) clearance on 2005-12-16. The listed applicant is Cosmedent, Inc.. The 510(k) number is K052263.

When did MULTIPLE (TOOTH DESENSITIZER) receive FDA 510(k) clearance?

MULTIPLE (TOOTH DESENSITIZER) received FDA 510(k) clearance on 2005-12-16, under 510(k) number K052263.

Who is the listed applicant for MULTIPLE (TOOTH DESENSITIZER)?

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 MULTIPLE (TOOTH DESENSITIZER)?

The FDA product code for MULTIPLE (TOOTH DESENSITIZER) is LBH.

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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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