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FDA 510(k)

TOKUYAMA BOND FORCE

K-Number: K070215 · 2007-03-30

ApplicantTokuyama Dental Corporation
Decision Date2007-03-30
Product CodeKLE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TOKUYAMA BOND FORCE is the device name listed in this FDA 510(k) record. The listed applicant is Tokuyama Dental Corporation. It received FDA 510(k) clearance on 2007-03-30 under 510(k) number K070215. 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 TOKUYAMA BOND FORCE?

TOKUYAMA BOND FORCE is a medical device that received FDA 510(k) clearance on 2007-03-30. The listed applicant is Tokuyama Dental Corporation. The 510(k) number is K070215.

When did TOKUYAMA BOND FORCE receive FDA 510(k) clearance?

TOKUYAMA BOND FORCE received FDA 510(k) clearance on 2007-03-30, under 510(k) number K070215.

Who is the listed applicant for TOKUYAMA BOND FORCE?

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

What is the FDA product code for TOKUYAMA BOND FORCE?

The FDA product code for TOKUYAMA BOND FORCE is KLE.

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Other records listing Tokuyama Dental Corporation 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.

K203760Tokuyama Universal Bond IIK203598Omnichroma Flow BulkK193537Omnichroma FlowK190940Tokuyama Rebase IIIK180613Estelite Universal FlowK173275OMNICHROMA

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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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