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FDA 510(k)

ZEODYNE TOOTHBRUSH WITH AGION ANTIMICROBIAL

K-Number: K021383 · 2002-07-17

ApplicantAgion Technologies, LLC
Decision Date2002-07-17
Product CodeEFW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ZEODYNE TOOTHBRUSH WITH AGION ANTIMICROBIAL is the device name listed in this FDA 510(k) record. The listed applicant is Agion Technologies, LLC. It received FDA 510(k) clearance on 2002-07-17 under 510(k) number K021383. 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 ZEODYNE TOOTHBRUSH WITH AGION ANTIMICROBIAL?

ZEODYNE TOOTHBRUSH WITH AGION ANTIMICROBIAL is a medical device that received FDA 510(k) clearance on 2002-07-17. The listed applicant is Agion Technologies, LLC. The 510(k) number is K021383.

When did ZEODYNE TOOTHBRUSH WITH AGION ANTIMICROBIAL receive FDA 510(k) clearance?

ZEODYNE TOOTHBRUSH WITH AGION ANTIMICROBIAL received FDA 510(k) clearance on 2002-07-17, under 510(k) number K021383.

Who is the listed applicant for ZEODYNE TOOTHBRUSH WITH AGION ANTIMICROBIAL?

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

What is the FDA product code for ZEODYNE TOOTHBRUSH WITH AGION ANTIMICROBIAL?

The FDA product code for ZEODYNE TOOTHBRUSH WITH AGION ANTIMICROBIAL is EFW.

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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 & GambleK020776MEDORAL HYGIENIC TOOTHBRUSH WITH DENTOSAN FILAMENTSCoronet Group North America, 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.

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