Eon Aligner
K-Number: K202685 · 2020-09-28
ApplicantEon Dental Jordan, LLC
Decision Date2020-09-28
Product CodeNXC
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Eon Aligner is a medical device manufactured by Eon Dental Jordan, LLC. It received FDA 510(k) clearance on 2020-09-28 under approval number K202685. 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 Eon Aligner?
Eon Aligner is a medical device that received FDA 510(k) clearance on 2020-09-28. It is manufactured by Eon Dental Jordan, LLC. The 510(k) number is K202685.
When was Eon Aligner approved by the FDA?
Eon Aligner received FDA 510(k) clearance on 2020-09-28, under approval number K202685.
What company makes Eon Aligner?
Eon Aligner is manufactured by Eon Dental Jordan, LLC.
What is the FDA product code for Eon Aligner?
The FDA product code for Eon Aligner 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.