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FDA 510(k)

WILDE ADHESIVE BONDING SYSTEM

K-Number: K913581 · 1993-02-26

ApplicantWilde-USA, Inc.
Decision Date1993-02-26
Product CodeKLE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

WILDE ADHESIVE BONDING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Wilde-USA, Inc.. It received FDA 510(k) clearance on 1993-02-26 under 510(k) number K913581. 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 WILDE ADHESIVE BONDING SYSTEM?

WILDE ADHESIVE BONDING SYSTEM is a medical device that received FDA 510(k) clearance on 1993-02-26. The listed applicant is Wilde-USA, Inc.. The 510(k) number is K913581.

When did WILDE ADHESIVE BONDING SYSTEM receive FDA 510(k) clearance?

WILDE ADHESIVE BONDING SYSTEM received FDA 510(k) clearance on 1993-02-26, under 510(k) number K913581.

Who is the listed applicant for WILDE ADHESIVE BONDING SYSTEM?

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

What is the FDA product code for WILDE ADHESIVE BONDING SYSTEM?

The FDA product code for WILDE ADHESIVE BONDING SYSTEM is KLE.

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Other records listing Wilde-USA, Inc. 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.

K913582COMPATIT RK915653KERAMAILK923472COMPACOLORK920649COMPASEPK915250WIL-PDS & WIL-PDI CASTING ALLOYSK913089WILDE LIGHT CURING COMPOSITE RESTORATIVE RESINS

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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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