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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is Changsha Honchon Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-07-08 under 510(k) 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. The listed applicant is Changsha Honchon Technology Co., Ltd.. The 510(k) number is K221051.

When did Dental Zirconia Blank & Dental Zirconia Pre-Shaded Blank receive FDA 510(k) clearance?

Dental Zirconia Blank & Dental Zirconia Pre-Shaded Blank received FDA 510(k) clearance on 2022-07-08, under 510(k) number K221051.

Who is the listed applicant for Dental Zirconia Blank & Dental Zirconia Pre-Shaded Blank?

The FDA 510(k) record lists Changsha Honchon Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

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 Devices (Code: EIH)

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

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