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FDA 510(k)

Magic Clear Aligners

K-Number: K190948 · 2019-05-09

ApplicantVoodoo Manufacturing, Inc.
Decision Date2019-05-09
Product CodeNXC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Magic Clear Aligners is the device name listed in this FDA 510(k) record. The listed applicant is Voodoo Manufacturing, Inc.. It received FDA 510(k) clearance on 2019-05-09 under 510(k) number K190948. 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 Magic Clear Aligners?

Magic Clear Aligners is a medical device that received FDA 510(k) clearance on 2019-05-09. The listed applicant is Voodoo Manufacturing, Inc.. The 510(k) number is K190948.

When did Magic Clear Aligners receive FDA 510(k) clearance?

Magic Clear Aligners received FDA 510(k) clearance on 2019-05-09, under 510(k) number K190948.

Who is the listed applicant for Magic Clear Aligners?

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

What is the FDA product code for Magic Clear Aligners?

The FDA product code for Magic Clear 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) 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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