Clear Aligner
K-Number: K213026 · 2022-08-16
Device Summary
Frequently Asked Questions
What is the Clear Aligner?
Clear Aligner is a medical device that received FDA 510(k) clearance on 2022-08-16. The listed applicant is Shenzhen Meiming Dentistry Technology Co., Ltd.. The 510(k) number is K213026.
When did Clear Aligner receive FDA 510(k) clearance?
Clear Aligner received FDA 510(k) clearance on 2022-08-16, under 510(k) number K213026.
Who is the listed applicant for Clear Aligner?
The FDA 510(k) record lists Shenzhen Meiming Dentistry Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Clear Aligner?
The FDA product code for Clear Aligner is NXC.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: NXC)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.