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FDA 510(k)

HERMES BOND

K-Number: K033974 · 2004-02-06

Applicant3M Espe AG Dental Products
Decision Date2004-02-06
Product CodeKLE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

HERMES BOND is the device name listed in this FDA 510(k) record. The listed applicant is 3M Espe AG Dental Products. It received FDA 510(k) clearance on 2004-02-06 under 510(k) number K033974. 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 HERMES BOND?

HERMES BOND is a medical device that received FDA 510(k) clearance on 2004-02-06. The listed applicant is 3M Espe AG Dental Products. The 510(k) number is K033974.

When did HERMES BOND receive FDA 510(k) clearance?

HERMES BOND received FDA 510(k) clearance on 2004-02-06, under 510(k) number K033974.

Who is the listed applicant for HERMES BOND?

The FDA 510(k) record lists 3M Espe AG Dental Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HERMES BOND?

The FDA product code for HERMES BOND is KLE.

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Other records listing 3M Espe AG Dental Products 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.

K100908UNICEM HMK100756MALTAK094007UNICEMK093721COSP2K091826ELEGANTK090718BELLUS SHADING KIT

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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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