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FDA 510(k)

Magic Clear Aligners

K-Number: K190948 · 2019-05-09

Decision Date2019-05-09
Product CodeNXC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Magic Clear Aligners is a medical device manufactured by Voodoo Manufacturing, Inc.. It received FDA 510(k) clearance on 2019-05-09 under approval 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. It is manufactured by Voodoo Manufacturing, Inc.. The 510(k) number is K190948.

When was Magic Clear Aligners approved by the FDA?

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

What company makes Magic Clear Aligners?

Magic Clear Aligners is manufactured by Voodoo Manufacturing, Inc..

What is the FDA product code for Magic Clear Aligners?

The FDA product code for Magic Clear Aligners is NXC.

Related Clinical Trials

Related Devices (Code: NXC)

Official Source

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