Dental Glass Ceramics Blocks
K-Number: K232438 · 2023-12-01
ApplicantAibodent Biotechnology Co., Ltd.
Decision Date2023-12-01
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Dental Glass Ceramics Blocks is a medical device manufactured by Aibodent Biotechnology Co., Ltd.. It received FDA 510(k) clearance on 2023-12-01 under approval number K232438. 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 Glass Ceramics Blocks?
Dental Glass Ceramics Blocks is a medical device that received FDA 510(k) clearance on 2023-12-01. It is manufactured by Aibodent Biotechnology Co., Ltd.. The 510(k) number is K232438.
When was Dental Glass Ceramics Blocks approved by the FDA?
Dental Glass Ceramics Blocks received FDA 510(k) clearance on 2023-12-01, under approval number K232438.
What company makes Dental Glass Ceramics Blocks?
Dental Glass Ceramics Blocks is manufactured by Aibodent Biotechnology Co., Ltd..
What is the FDA product code for Dental Glass Ceramics Blocks?
The FDA product code for Dental Glass Ceramics Blocks is EIH.
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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.