Dental Glass Ceramics Blocks
K-Number: K232438 · 2023-12-01
Device Summary
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. The listed applicant is Aibodent Biotechnology Co., Ltd.. The 510(k) number is K232438.
When did Dental Glass Ceramics Blocks receive FDA 510(k) clearance?
Dental Glass Ceramics Blocks received FDA 510(k) clearance on 2023-12-01, under 510(k) number K232438.
Who is the listed applicant for Dental Glass Ceramics Blocks?
The FDA 510(k) record lists Aibodent Biotechnology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Dental Glass Ceramics Blocks?
The FDA product code for Dental Glass Ceramics Blocks is EIH.
Related Clinical Trials
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.