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FDA 510(k)

AMARIS/AMARIS FLOW

K-Number: K071386 · 2007-06-05

ApplicantVoco GmbH
Decision Date2007-06-05
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

AMARIS/AMARIS FLOW is the device name listed in this FDA 510(k) record. The listed applicant is Voco GmbH. It received FDA 510(k) clearance on 2007-06-05 under 510(k) number K071386. 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 AMARIS/AMARIS FLOW?

AMARIS/AMARIS FLOW is a medical device that received FDA 510(k) clearance on 2007-06-05. The listed applicant is Voco GmbH. The 510(k) number is K071386.

When did AMARIS/AMARIS FLOW receive FDA 510(k) clearance?

AMARIS/AMARIS FLOW received FDA 510(k) clearance on 2007-06-05, under 510(k) number K071386.

Who is the listed applicant for AMARIS/AMARIS FLOW?

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

What is the FDA product code for AMARIS/AMARIS FLOW?

The FDA product code for AMARIS/AMARIS FLOW is EBF.

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Other records listing Voco GmbH 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.

K252073VOCO Profluorid Varnish + BioMinK261357Grandio disc multicolorK252606Bifix Veneer LC, Bifix Veneer Try-InK251390MTA vptK251239GrandioSO UnlimitedK231817AlignerFlow LC

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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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