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FDA 510(k)

BEAUTIBOND MULTI PR PLUS

K-Number: K110252 · 2011-05-13

ApplicantShofu Dental Corp.
Decision Date2011-05-13
Product CodeKLE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BEAUTIBOND MULTI PR PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Shofu Dental Corp.. It received FDA 510(k) clearance on 2011-05-13 under 510(k) number K110252. 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 BEAUTIBOND MULTI PR PLUS?

BEAUTIBOND MULTI PR PLUS is a medical device that received FDA 510(k) clearance on 2011-05-13. The listed applicant is Shofu Dental Corp.. The 510(k) number is K110252.

When did BEAUTIBOND MULTI PR PLUS receive FDA 510(k) clearance?

BEAUTIBOND MULTI PR PLUS received FDA 510(k) clearance on 2011-05-13, under 510(k) number K110252.

Who is the listed applicant for BEAUTIBOND MULTI PR PLUS?

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

What is the FDA product code for BEAUTIBOND MULTI PR PLUS?

The FDA product code for BEAUTIBOND MULTI PR PLUS is KLE.

Related Clinical Trials

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Other records listing Shofu Dental Corp. 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.

K111855HY-BOND RESIGLASSK110235BEAUTIBOND MULTIK101603BEAUTIFIL FLOW PLUSK101621LITE ARTK093559VINTAGE MPK082744BEAUTIBOND

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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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