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FDA 510(k)

MVP Aligner System

K-Number: K193130 · 2020-08-07

ApplicantMvp Aligners, LLC
Decision Date2020-08-07
Product CodeNXC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MVP Aligner System is the device name listed in this FDA 510(k) record. The listed applicant is Mvp Aligners, LLC. It received FDA 510(k) clearance on 2020-08-07 under 510(k) number K193130. 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 MVP Aligner System?

MVP Aligner System is a medical device that received FDA 510(k) clearance on 2020-08-07. The listed applicant is Mvp Aligners, LLC. The 510(k) number is K193130.

When did MVP Aligner System receive FDA 510(k) clearance?

MVP Aligner System received FDA 510(k) clearance on 2020-08-07, under 510(k) number K193130.

Who is the listed applicant for MVP Aligner System?

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

What is the FDA product code for MVP Aligner System?

The FDA product code for MVP Aligner System 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) LimitedK250739Primeprint Direct AlignerDreve Dentamid GmbH

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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