Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MEDORAL HYGIENIC TOOTHBRUSH WITH DENTOSAN FILAMENTS

K-Number: K020776 · 2002-06-03

ApplicantCoronet Group North America, LLC
Decision Date2002-06-03
Product CodeEFW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MEDORAL HYGIENIC TOOTHBRUSH WITH DENTOSAN FILAMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Coronet Group North America, LLC. It received FDA 510(k) clearance on 2002-06-03 under 510(k) number K020776. The device is classified under product code EFW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDORAL HYGIENIC TOOTHBRUSH WITH DENTOSAN FILAMENTS?

MEDORAL HYGIENIC TOOTHBRUSH WITH DENTOSAN FILAMENTS is a medical device that received FDA 510(k) clearance on 2002-06-03. The listed applicant is Coronet Group North America, LLC. The 510(k) number is K020776.

When did MEDORAL HYGIENIC TOOTHBRUSH WITH DENTOSAN FILAMENTS receive FDA 510(k) clearance?

MEDORAL HYGIENIC TOOTHBRUSH WITH DENTOSAN FILAMENTS received FDA 510(k) clearance on 2002-06-03, under 510(k) number K020776.

Who is the listed applicant for MEDORAL HYGIENIC TOOTHBRUSH WITH DENTOSAN FILAMENTS?

The FDA 510(k) record lists Coronet Group North America, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDORAL HYGIENIC TOOTHBRUSH WITH DENTOSAN FILAMENTS?

The FDA product code for MEDORAL HYGIENIC TOOTHBRUSH WITH DENTOSAN FILAMENTS is EFW.

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

Related Devices (Code: EFW)

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.

K130186DENTEK EASY BRUSH WITH FLUORIDEDen Tek Oral Care, Inc.K121165BEAM BRUSH/BEAM APPBeam Technologies, LLCK102871SILVER CARE ANITBACTERIAL TOOTHBRUSHPiave Spazzolificio S.P.A.K073224ORAL-B SUB-BRAND MANUAL TOOTHBRUSHProcter & GambleK021383ZEODYNE TOOTHBRUSH WITH AGION ANTIMICROBIALAgion Technologies, LLCK000290LAZERSMILE, LAZERWHITEBiolase Technology, 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.

↑