Illusion Aligner Pro: Illusion Aligner FLX
K-Number: K233356 · 2024-08-08
ApplicantLaxmi Dental Export Pvt., Ltd.
Decision Date2024-08-08
Product CodeNXC
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Illusion Aligner Pro: Illusion Aligner FLX is a medical device manufactured by Laxmi Dental Export Pvt., Ltd.. It received FDA 510(k) clearance on 2024-08-08 under approval number K233356. 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 Aligner Pro: Illusion Aligner FLX?
Illusion Aligner Pro: Illusion Aligner FLX is a medical device that received FDA 510(k) clearance on 2024-08-08. It is manufactured by Laxmi Dental Export Pvt., Ltd.. The 510(k) number is K233356.
When was Illusion Aligner Pro: Illusion Aligner FLX approved by the FDA?
Illusion Aligner Pro: Illusion Aligner FLX received FDA 510(k) clearance on 2024-08-08, under approval number K233356.
What company makes Illusion Aligner Pro: Illusion Aligner FLX?
Illusion Aligner Pro: Illusion Aligner FLX is manufactured by Laxmi Dental Export Pvt., Ltd..
What is the FDA product code for Illusion Aligner Pro: Illusion Aligner FLX?
The FDA product code for Illusion Aligner Pro: Illusion Aligner FLX 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.