Dental Zirconia Blank & Dental Zirconia Pre-Shaded Blank
K-Number: K221051 · 2022-07-08
Decision Date2022-07-08
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Dental Zirconia Blank & Dental Zirconia Pre-Shaded Blank is a medical device manufactured by Changsha Honchon Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-07-08 under approval number K221051. 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 Blank & Dental Zirconia Pre-Shaded Blank?
Dental Zirconia Blank & Dental Zirconia Pre-Shaded Blank is a medical device that received FDA 510(k) clearance on 2022-07-08. It is manufactured by Changsha Honchon Technology Co., Ltd.. The 510(k) number is K221051.
When was Dental Zirconia Blank & Dental Zirconia Pre-Shaded Blank approved by the FDA?
Dental Zirconia Blank & Dental Zirconia Pre-Shaded Blank received FDA 510(k) clearance on 2022-07-08, under approval number K221051.
What company makes Dental Zirconia Blank & Dental Zirconia Pre-Shaded Blank?
Dental Zirconia Blank & Dental Zirconia Pre-Shaded Blank is manufactured by Changsha Honchon Technology Co., Ltd..
What is the FDA product code for Dental Zirconia Blank & Dental Zirconia Pre-Shaded Blank?
The FDA product code for Dental Zirconia Blank & Dental Zirconia Pre-Shaded Blank is EIH.
Related Clinical Trials
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.