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FDA 510(k)

FLOWABLE COMPOSITE/ ECUFLOW/ LUXAFLOW

K-Number: K011211 · 2001-06-18

ApplicantDmg USA, Inc.
Decision Date2001-06-18
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FLOWABLE COMPOSITE/ ECUFLOW/ LUXAFLOW is the device name listed in this FDA 510(k) record. The listed applicant is Dmg USA, Inc.. It received FDA 510(k) clearance on 2001-06-18 under 510(k) number K011211. 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 FLOWABLE COMPOSITE/ ECUFLOW/ LUXAFLOW?

FLOWABLE COMPOSITE/ ECUFLOW/ LUXAFLOW is a medical device that received FDA 510(k) clearance on 2001-06-18. The listed applicant is Dmg USA, Inc.. The 510(k) number is K011211.

When did FLOWABLE COMPOSITE/ ECUFLOW/ LUXAFLOW receive FDA 510(k) clearance?

FLOWABLE COMPOSITE/ ECUFLOW/ LUXAFLOW received FDA 510(k) clearance on 2001-06-18, under 510(k) number K011211.

Who is the listed applicant for FLOWABLE COMPOSITE/ ECUFLOW/ LUXAFLOW?

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

What is the FDA product code for FLOWABLE COMPOSITE/ ECUFLOW/ LUXAFLOW?

The FDA product code for FLOWABLE COMPOSITE/ ECUFLOW/ LUXAFLOW is EBF.

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.

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Other records listing Dmg USA, 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.

K171772Ecosite Bulk FillK160443TempoCem ClearK110759TEMPOCEMK102603SA FLOWABLE ADHESIVEK101710LUXATEMP ULTRA /STARK100062INFILTRATION KIT

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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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