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FDA 510(k)

ADHESIVE DC ACTIVATOR

K-Number: K062713 · 2006-11-02

ApplicantIvoclar Vivadent, Inc.
Decision Date2006-11-02
Product CodeKLE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ADHESIVE DC ACTIVATOR is the device name listed in this FDA 510(k) record. The listed applicant is Ivoclar Vivadent, Inc.. It received FDA 510(k) clearance on 2006-11-02 under 510(k) number K062713. 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 ADHESIVE DC ACTIVATOR?

ADHESIVE DC ACTIVATOR is a medical device that received FDA 510(k) clearance on 2006-11-02. The listed applicant is Ivoclar Vivadent, Inc.. The 510(k) number is K062713.

When did ADHESIVE DC ACTIVATOR receive FDA 510(k) clearance?

ADHESIVE DC ACTIVATOR received FDA 510(k) clearance on 2006-11-02, under 510(k) number K062713.

Who is the listed applicant for ADHESIVE DC ACTIVATOR?

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

What is the FDA product code for ADHESIVE DC ACTIVATOR?

The FDA product code for ADHESIVE DC ACTIVATOR is KLE.

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Other records listing Ivoclar Vivadent, Inc. as applicant

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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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