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FDA 510(k)

QUICKSMILE

K-Number: K052040 · 2005-10-18

ApplicantCosmetic Dental Materials, Inc.
Decision Date2005-10-18
Product CodeEEG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

QUICKSMILE is the device name listed in this FDA 510(k) record. The listed applicant is Cosmetic Dental Materials, Inc.. It received FDA 510(k) clearance on 2005-10-18 under 510(k) number K052040. The device is classified under product code EEG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUICKSMILE?

QUICKSMILE is a medical device that received FDA 510(k) clearance on 2005-10-18. The listed applicant is Cosmetic Dental Materials, Inc.. The 510(k) number is K052040.

When did QUICKSMILE receive FDA 510(k) clearance?

QUICKSMILE received FDA 510(k) clearance on 2005-10-18, under 510(k) number K052040.

Who is the listed applicant for QUICKSMILE?

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

What is the FDA product code for QUICKSMILE?

The FDA product code for QUICKSMILE is EEG.

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.

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Other records listing Cosmetic Dental Materials, 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.

K063626DURAFLEX

Related Devices (Code: EEG)

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.

K122725TANDA PEARL, ULTRAWYTE, PEARLSyneron BeautyK110888ABSOLUTE WHITE LIGHTDr. Fresh, Inc.K063704BRITEWHITE TEETH WHITENING SYSTEM, MODEL BW1101Beks IncorporatedK042153SOUTH BEACH SMILE LIGHT WHITENING SYSTEMDentovations, Inc.K041392SONX 35 ULTRASONIC BLEACHING SYSTEM; SONIWHITE ULTRA SONIC, MODEL QUICK WHITE USCAO Group, Inc.K895174UNION BROACH BLEACHING LIGHTUnion Broach, Div. Moyco Industries, Inc.

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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