Clear Aligner
K-Number: K213026 · 2022-08-16
Decision Date2022-08-16
Product CodeNXC
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Clear Aligner is a medical device manufactured by Shenzhen Meiming Dentistry Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-08-16 under approval number K213026. 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 Clear Aligner?
Clear Aligner is a medical device that received FDA 510(k) clearance on 2022-08-16. It is manufactured by Shenzhen Meiming Dentistry Technology Co., Ltd.. The 510(k) number is K213026.
When was Clear Aligner approved by the FDA?
Clear Aligner received FDA 510(k) clearance on 2022-08-16, under approval number K213026.
What company makes Clear Aligner?
Clear Aligner is manufactured by Shenzhen Meiming Dentistry Technology Co., Ltd..
What is the FDA product code for Clear Aligner?
The FDA product code for Clear Aligner is NXC.
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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.