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FDA 510(k)

DENTOLOCK DENTURE ADHESIVE CREAM

K-Number: K831265 · 1983-05-09

ApplicantSolar Dental Co., Inc.
Decision Date1983-05-09
Product CodeKOQ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTOLOCK DENTURE ADHESIVE CREAM 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 1983-05-09 under 510(k) number K831265. The device is classified under product code KOQ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTOLOCK DENTURE ADHESIVE CREAM?

DENTOLOCK DENTURE ADHESIVE CREAM is a medical device that received FDA 510(k) clearance on 1983-05-09. The listed applicant is Solar Dental Co., Inc.. The 510(k) number is K831265.

When did DENTOLOCK DENTURE ADHESIVE CREAM receive FDA 510(k) clearance?

DENTOLOCK DENTURE ADHESIVE CREAM received FDA 510(k) clearance on 1983-05-09, under 510(k) number K831265.

Who is the listed applicant for DENTOLOCK DENTURE ADHESIVE CREAM?

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 DENTOLOCK DENTURE ADHESIVE CREAM?

The FDA product code for DENTOLOCK DENTURE ADHESIVE CREAM is KOQ.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K871980D-23 DENTURE ADHESIVEK861846HYDRON ROOT CANAL FILLING & MARK IV STARTER KITK852926DENTOLOCK II DENTURE ADHESIVE CREAMK831294SOLARCRY/TEMPORARY CROWN & BRIDGE MATK831293SOLARCRYL CUSTOM TRAY MATERIAL

Related Devices (Code: KOQ)

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.

K901882URESIL ENDOSCOPIC LASER OVERTUBEUresil Corp.K896821OLYMPUS URETERO. & CIRCON ACMI URETERO. GUIDENorth American Sterilization & Packaging Co.K900401NAS&P GRASPING FORCEPS & ASSOC. DEVICESNorth American Sterilization & Packaging Co.

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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