FDA 510(k)

Concinnity Aligners

K-Number: K200005 · 2020-11-09

ApplicantDrake Precision Dental Laboratory, Inc.

Decision Date2020-11-09

Product CodeNXC

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

Concinnity Aligners is the device name listed in this FDA 510(k) record. The listed applicant is Drake Precision Dental Laboratory, Inc.. It received FDA 510(k) clearance on 2020-11-09 under 510(k) number K200005. The device is classified under product code NXC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Concinnity Aligners?

Concinnity Aligners is a medical device that received FDA 510(k) clearance on 2020-11-09. The listed applicant is Drake Precision Dental Laboratory, Inc.. The 510(k) number is K200005.

When did Concinnity Aligners receive FDA 510(k) clearance?

Concinnity Aligners received FDA 510(k) clearance on 2020-11-09, under 510(k) number K200005.

Who is the listed applicant for Concinnity Aligners?

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

What is the FDA product code for Concinnity Aligners?

The FDA product code for Concinnity Aligners is NXC.

Related Devices (Code: NXC)

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.

K260527FACE4D AlignerAvinent Implant System S.L.U.K260788Smylio AlignersSmylio, Inc.K260722SureSmile Aligner (ASSY500020)Dentsply Sirona, Inc.K253282ZSmile SystemDror Orthodesign , Ltd.K251454Clear Aligner (SCF-3348)Beame Medical Technology (Shenzhen) Limited K250739Primeprint Direct AlignerDreve Dentamid GmbH

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.