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FDA 510(k)

ADHESIVE EXL-759

K-Number: K110302 · 2011-05-19

Applicant3M Espe AG
Decision Date2011-05-19
Product CodeKLE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ADHESIVE EXL-759 is the device name listed in this FDA 510(k) record. The listed applicant is 3M Espe AG. It received FDA 510(k) clearance on 2011-05-19 under 510(k) number K110302. 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 EXL-759?

ADHESIVE EXL-759 is a medical device that received FDA 510(k) clearance on 2011-05-19. The listed applicant is 3M Espe AG. The 510(k) number is K110302.

When did ADHESIVE EXL-759 receive FDA 510(k) clearance?

ADHESIVE EXL-759 received FDA 510(k) clearance on 2011-05-19, under 510(k) number K110302.

Who is the listed applicant for ADHESIVE EXL-759?

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

What is the FDA product code for ADHESIVE EXL-759?

The FDA product code for ADHESIVE EXL-759 is KLE.

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Other records listing 3M Espe AG 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.

K120011HEISENBERG EFFECT SHADESK110508SUGLUE-10K111257HEISENBERG DYEING LIQUIDS

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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