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FDA 510(k)

PREMIER SELF-ETCHING BOND ENHANCER

K-Number: K061998 · 2006-10-04

ApplicantPremier Dental Products Co.
Decision Date2006-10-04
Product CodeKLE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PREMIER SELF-ETCHING BOND ENHANCER is the device name listed in this FDA 510(k) record. The listed applicant is Premier Dental Products Co.. It received FDA 510(k) clearance on 2006-10-04 under 510(k) number K061998. 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 PREMIER SELF-ETCHING BOND ENHANCER?

PREMIER SELF-ETCHING BOND ENHANCER is a medical device that received FDA 510(k) clearance on 2006-10-04. The listed applicant is Premier Dental Products Co.. The 510(k) number is K061998.

When did PREMIER SELF-ETCHING BOND ENHANCER receive FDA 510(k) clearance?

PREMIER SELF-ETCHING BOND ENHANCER received FDA 510(k) clearance on 2006-10-04, under 510(k) number K061998.

Who is the listed applicant for PREMIER SELF-ETCHING BOND ENHANCER?

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

What is the FDA product code for PREMIER SELF-ETCHING BOND ENHANCER?

The FDA product code for PREMIER SELF-ETCHING BOND ENHANCER is KLE.

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Other records listing Premier 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.

K132526KNIT-PAK+K131212PREMIER CERAMIC PRIMERK083695TRAXODENTK062683ENAMEL PRO VARNISHK062166ENAMEL PROK061997PREMIER SELF-ETCHING ENAMEL SEALANT

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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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