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FDA 510(k)

BENDA BRUSH

K-Number: K885162 · 1989-01-10

ApplicantCentrix, Inc.
Decision Date1989-01-10
Product CodeEKJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BENDA BRUSH is the device name listed in this FDA 510(k) record. The listed applicant is Centrix, Inc.. It received FDA 510(k) clearance on 1989-01-10 under 510(k) number K885162. The device is classified under product code EKJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BENDA BRUSH?

BENDA BRUSH is a medical device that received FDA 510(k) clearance on 1989-01-10. The listed applicant is Centrix, Inc.. The 510(k) number is K885162.

When did BENDA BRUSH receive FDA 510(k) clearance?

BENDA BRUSH received FDA 510(k) clearance on 1989-01-10, under 510(k) number K885162.

Who is the listed applicant for BENDA BRUSH?

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

What is the FDA product code for BENDA BRUSH?

The FDA product code for BENDA BRUSH is EKJ.

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Other records listing Centrix, 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.

K250714FluoroDose VarnishK222459Centrix FluoroSilver Silver Diamine Fluoride 38%K152826NoCordK120176SENZZZZZ AWAYK111348RE / STASIS (TM) GINGIVAL RETRACTION PASTEK092384LIQUICORD

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Related Devices (Code: EKJ)

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.

K961714ASEPTYLUM, UNI-CARRIERDistriflor S.A.K953707MEDTROL DENTAL KITMedtrol, Inc.K945815DENTAL KITConstancy Ent., Inc.K951607SUREFLEX FILESDentsply Intl.K945077INSTRUMENT,FILLING,PLASTIC,DENTALWorldwide Dental, Inc.K943820STAT PAKMagnum Instruments, 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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