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FDA 510(k)

ETCHANT 40%

K-Number: K030743 · 2003-05-09

ApplicantConfi-Dental Products Co.
Decision Date2003-05-09
Product CodeKLE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ETCHANT 40% is the device name listed in this FDA 510(k) record. The listed applicant is Confi-Dental Products Co.. It received FDA 510(k) clearance on 2003-05-09 under 510(k) number K030743. The device is classified under product code KLE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ETCHANT 40%?

ETCHANT 40% is a medical device that received FDA 510(k) clearance on 2003-05-09. The listed applicant is Confi-Dental Products Co.. The 510(k) number is K030743.

When did ETCHANT 40% receive FDA 510(k) clearance?

ETCHANT 40% received FDA 510(k) clearance on 2003-05-09, under 510(k) number K030743.

Who is the listed applicant for ETCHANT 40%?

The FDA 510(k) record lists Confi-Dental Products Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ETCHANT 40%?

The FDA product code for ETCHANT 40% is KLE.

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Other records listing Confi-Dental Products Co. 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.

K030807CARIES INDICATORK955328CONFI-BONDK955329RESILIENCE M5 PROTECTION PLUSK954988CRYSTALLESSENCEK952930DENTRAY II PLUS TRAY ADHESIVEK946307CYRSTALLINE L3 MULTI-USE HYBRID COMPOSITE

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Related Devices (Code: KLE)

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.

K262252MPa Max adhesiveDen-Mat Holdings, LLCK260485Any-EtchMediclus Co., Ltd.K260430Porcelain Etch GelBelport Company, Inc., Gingi-PakK252450Adhese 2Ivoclar Vivadent, Inc.K260682Bond-PR™ Universal AdhesivePremier Dental Products CompanyK251587VITA VMLC PrimerVita Zahnfabrik H. Rauter GmbH & Co. Kg.

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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