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FDA 510(k)

D-23 DENTURE ADHESIVE

K-Number: K871980 · 1987-06-05

ApplicantSolar Dental Co., Inc.
Decision Date1987-06-05
Product CodeKOJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

D-23 DENTURE ADHESIVE is the device name listed in this FDA 510(k) record. The listed applicant is Solar Dental Co., Inc.. It received FDA 510(k) clearance on 1987-06-05 under 510(k) number K871980. The device is classified under product code KOJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the D-23 DENTURE ADHESIVE?

D-23 DENTURE ADHESIVE is a medical device that received FDA 510(k) clearance on 1987-06-05. The listed applicant is Solar Dental Co., Inc.. The 510(k) number is K871980.

When did D-23 DENTURE ADHESIVE receive FDA 510(k) clearance?

D-23 DENTURE ADHESIVE received FDA 510(k) clearance on 1987-06-05, under 510(k) number K871980.

Who is the listed applicant for D-23 DENTURE ADHESIVE?

The FDA 510(k) record lists Solar Dental Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for D-23 DENTURE ADHESIVE?

The FDA product code for D-23 DENTURE ADHESIVE is KOJ.

Related Clinical Trials

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Other records listing Solar Dental Co., 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.

K861846HYDRON ROOT CANAL FILLING & MARK IV STARTER KITK852926DENTOLOCK II DENTURE ADHESIVE CREAMK831294SOLARCRY/TEMPORARY CROWN & BRIDGE MATK831293SOLARCRYL CUSTOM TRAY MATERIALK831265DENTOLOCK DENTURE ADHESIVE CREAM

Related Devices (Code: KOJ)

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.

K251425turbodent touchMectron S.P.A.K063236BETA-POWDERBrainbase CorporationK042872RONDOFLEX PLUS 360Kavo America CorporationK033675PROSMILE AIR POLISHER AND PROPHYLAXIS POWDERSirona Dental Systems GmbHK033215PREPAIRDanville Materials, Inc.K024105VELOPEX AQUACUT FLUID ABRASION UNITVelopex International, Inc.

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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