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FDA 510(k)

BEAM BRUSH/BEAM APP

K-Number: K121165 · 2012-06-21

ApplicantBeam Technologies, LLC
Decision Date2012-06-21
Product CodeEFW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BEAM BRUSH/BEAM APP is the device name listed in this FDA 510(k) record. The listed applicant is Beam Technologies, LLC. It received FDA 510(k) clearance on 2012-06-21 under 510(k) number K121165. 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 BEAM BRUSH/BEAM APP?

BEAM BRUSH/BEAM APP is a medical device that received FDA 510(k) clearance on 2012-06-21. The listed applicant is Beam Technologies, LLC. The 510(k) number is K121165.

When did BEAM BRUSH/BEAM APP receive FDA 510(k) clearance?

BEAM BRUSH/BEAM APP received FDA 510(k) clearance on 2012-06-21, under 510(k) number K121165.

Who is the listed applicant for BEAM BRUSH/BEAM APP?

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

What is the FDA product code for BEAM BRUSH/BEAM APP?

The FDA product code for BEAM BRUSH/BEAM APP 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.K102871SILVER CARE ANITBACTERIAL TOOTHBRUSHPiave Spazzolificio S.P.A.K073224ORAL-B SUB-BRAND MANUAL TOOTHBRUSHProcter & GambleK021383ZEODYNE TOOTHBRUSH WITH AGION ANTIMICROBIALAgion Technologies, LLCK020776MEDORAL 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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