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)

Dental Zirconia Ceramic

K-Number: K222626 · 2022-12-06

Decision Date2022-12-06
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Dental Zirconia Ceramic is a medical device manufactured by Aidite (Qinhuangdao) Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-12-06 under approval number K222626. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Dental Zirconia Ceramic?

Dental Zirconia Ceramic is a medical device that received FDA 510(k) clearance on 2022-12-06. It is manufactured by Aidite (Qinhuangdao) Technology Co., Ltd.. The 510(k) number is K222626.

When was Dental Zirconia Ceramic approved by the FDA?

Dental Zirconia Ceramic received FDA 510(k) clearance on 2022-12-06, under approval number K222626.

What company makes Dental Zirconia Ceramic?

Dental Zirconia Ceramic is manufactured by Aidite (Qinhuangdao) Technology Co., Ltd..

What is the FDA product code for Dental Zirconia Ceramic?

The FDA product code for Dental Zirconia Ceramic is EIH.

Related Clinical Trials

Other Devices by Aidite (Qinhuangdao) Technology Co., Ltd.

View all 16 devices →

Related Devices (Code: EIH)

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.