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FDA 510(k)

DMC COMPOSITE

K-Number: K081695 · 2008-08-12

ApplicantKerr Corp.
Decision Date2008-08-12
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DMC COMPOSITE is the device name listed in this FDA 510(k) record. The listed applicant is Kerr Corp.. It received FDA 510(k) clearance on 2008-08-12 under 510(k) number K081695. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DMC COMPOSITE?

DMC COMPOSITE is a medical device that received FDA 510(k) clearance on 2008-08-12. The listed applicant is Kerr Corp.. The 510(k) number is K081695.

When did DMC COMPOSITE receive FDA 510(k) clearance?

DMC COMPOSITE received FDA 510(k) clearance on 2008-08-12, under 510(k) number K081695.

Who is the listed applicant for DMC COMPOSITE?

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

What is the FDA product code for DMC COMPOSITE?

The FDA product code for DMC COMPOSITE is EBF.

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Other records listing Kerr Corp. 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.

K091613TAKE 1K090292PREMISE MODIFIEDK072622STANDOUT 2K042888DEMETRON IDS CURING LIGHTK031484STAND OUTK014179DEMETRON LC

View all 9 devices →

Related Devices (Code: EBF)

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.

K262982Core·it DualSpident Co., Ltd.K262202Cerasmart ForteGC America, Inc.K261695Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF)Guilin Kevin Peter Technology Co., Ltd.K261485Tetric plus Fill;Tetric plus FlowIvoclar Vivadent, Inc.K262228Transcend Bulk Fill Flowable CompositeUltradent Products, Inc.K261246SRGC-06GC America, 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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