Dental Porcelain Powder
K-Number: K232676 · 2024-01-23
Decision Date2024-01-23
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Dental Porcelain Powder is a medical device manufactured by Chengdu Besmile Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-01-23 under approval number K232676. 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 Porcelain Powder?
Dental Porcelain Powder is a medical device that received FDA 510(k) clearance on 2024-01-23. It is manufactured by Chengdu Besmile Medical Technology Co., Ltd.. The 510(k) number is K232676.
When was Dental Porcelain Powder approved by the FDA?
Dental Porcelain Powder received FDA 510(k) clearance on 2024-01-23, under approval number K232676.
What company makes Dental Porcelain Powder?
Dental Porcelain Powder is manufactured by Chengdu Besmile Medical Technology Co., Ltd..
What is the FDA product code for Dental Porcelain Powder?
The FDA product code for Dental Porcelain Powder is EIH.
Related Clinical Trials
Other Devices by Chengdu Besmile Medical Technology Co., Ltd.
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.