Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Illusion Aligners

K-Number: K211010 · 2021-04-26

Decision Date2021-04-26
Product CodeNXC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Illusion Aligners is a medical device manufactured by Laxmi Dental Exports Pvt, Ltd.. It received FDA 510(k) clearance on 2021-04-26 under approval number K211010. 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 Illusion Aligners?

Illusion Aligners is a medical device that received FDA 510(k) clearance on 2021-04-26. It is manufactured by Laxmi Dental Exports Pvt, Ltd.. The 510(k) number is K211010.

When was Illusion Aligners approved by the FDA?

Illusion Aligners received FDA 510(k) clearance on 2021-04-26, under approval number K211010.

What company makes Illusion Aligners?

Illusion Aligners is manufactured by Laxmi Dental Exports Pvt, Ltd..

What is the FDA product code for Illusion Aligners?

The FDA product code for Illusion Aligners is NXC.

Related Devices (Code: NXC)

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.