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FDA 510(k)

DMP SINGLE BONDING

K-Number: K102254 · 2010-11-23

ApplicantDmp, Ltd.
Decision Date2010-11-23
Product CodeKLE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DMP SINGLE BONDING is the device name listed in this FDA 510(k) record. The listed applicant is Dmp, Ltd.. It received FDA 510(k) clearance on 2010-11-23 under 510(k) number K102254. 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 DMP SINGLE BONDING?

DMP SINGLE BONDING is a medical device that received FDA 510(k) clearance on 2010-11-23. The listed applicant is Dmp, Ltd.. The 510(k) number is K102254.

When did DMP SINGLE BONDING receive FDA 510(k) clearance?

DMP SINGLE BONDING received FDA 510(k) clearance on 2010-11-23, under 510(k) number K102254.

Who is the listed applicant for DMP SINGLE BONDING?

The FDA 510(k) record lists Dmp, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DMP SINGLE BONDING?

The FDA product code for DMP SINGLE BONDING is KLE.

Related Clinical Trials

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.

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Other records listing Dmp, Ltd. 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.

K121915BRIGHT RESTORATIVE MATERIALSK102836BONASIL A+ IMPRESSION MATERIALSK102252DMP PIT & FISSURE SEALANTK102255DMP ETCHING GELK102257NANOCERAM- BRIGHT

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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