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FDA 510(k)

KERR ADVANCED ADHESIVE

K-Number: K962515 · 1996-08-01

ApplicantKerr Dental Materials Center
Decision Date1996-08-01
Product CodeKLE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

KERR ADVANCED ADHESIVE is the device name listed in this FDA 510(k) record. The listed applicant is Kerr Dental Materials Center. It received FDA 510(k) clearance on 1996-08-01 under 510(k) number K962515. 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 KERR ADVANCED ADHESIVE?

KERR ADVANCED ADHESIVE is a medical device that received FDA 510(k) clearance on 1996-08-01. The listed applicant is Kerr Dental Materials Center. The 510(k) number is K962515.

When did KERR ADVANCED ADHESIVE receive FDA 510(k) clearance?

KERR ADVANCED ADHESIVE received FDA 510(k) clearance on 1996-08-01, under 510(k) number K962515.

Who is the listed applicant for KERR ADVANCED ADHESIVE?

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

What is the FDA product code for KERR ADVANCED ADHESIVE?

The FDA product code for KERR ADVANCED ADHESIVE is KLE.

Related Clinical Trials

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Other records listing Kerr Dental Materials Center 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.

K050984BIOPLANTK031444OPTIBOND FLK030646BELLEGLASS POINT 4K020303XR PRIMER 2K020178BELLEGLASS HP MODELING GELK014027OPTIBOND SOLO PLUS 4

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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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